CAS: 830-79-5; 2,4,6-Trimethoxybenzaldehyde

该化合物是一种替代苯甲醚衍生物,其特点是在芳香环的2,4和6个位置上有三个甲氧基组,该化合物是有机合成的多用途中间体,特别是在制备药品,农用化学品和精美化学品方面.其电子富含芳香的结构增强了电益替代和凝聚反应中的回活动.甲氧基组有助于产生消毒和电子效应,影响合成途径的选择性.化合物在标准条件下表现出稳定性,在普通有机溶剂中可溶解,便于在多步反应中使用.其定义明确的结构对于在药用和材料化学研究中构建复杂的分子很有价值.

英文名称2,4,6-Trimethoxybenzaldehyde
中文名称2,4,6-三甲氧基苯甲醛
IUPAC名称2,4,6-trimethoxybenzaldehyde
其它别名2,4,6-三甲氧基苯(甲)醛; 246三甲氧基苯甲醛; 2,4,6-Trimethoxybenzaldehyde
CAS编号830-79-5
MFCD编号:MFCD00003313
EINECS号:212-598-2
FDA UNII编号:JD365X6J84
分子式:C10H12O4
分子量:196.2
产品CID: 1820114
产品分类有机原料→分子砌块→芳环类化合物→苯类化合物

相似结构搜索
产品信息参考;;;;
InChIKey: CRBZVDLXAIFERF-UHFFFAOYSA-N
InChI=1S/C10H12O4/c1-12-7-4-9(13-2)8(6-11)10(5-7)14-3/h4-6H,1-3H3…
计算化学: 氢键受体数4.0氢键供体数0.0可旋转键数4.0

物理性质

熔点115-120°C
沸点339.1°C at 760 mmHg
闪点151.3±26.5 °C
密度1.1±0.1 g/cm3
PSA:44.76
LogP:1.5249
折射率1.525
蒸汽压0.0±0.7 mmHg at 25°C
溶解性Chloroform (Slightly), Methanol (Slightly)
敏感性空气敏感
外观形态米色结晶粉末
储存条件置于阴暗处,密封, 常温干燥保存
产品应用该化合物用于新的(+/-)-8-ALKYL-57-二氧氧基-4-(4-羟基苯)-34-二氢基辛基氨的转基因选择性合成的试剂.
性质描述熔点118-120°C

MSDS等安全信息

GHS象形图
GHS符号GHS07;
注释: Exclamation mark
危险类别特定目标器官毒性 - 单次接触类别3
皮肤腐蚀/刺激类别2
严重眼刺激类别2A
严重眼刺激类别2
警示词Warning(警告)
危险描述H335 |可能引起呼吸道刺激.
H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
防范说明P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
UN编号NONH for all modes of transport
危险品标志C
安全声明22-24/25-45-36/37/39-27-26
危险类别码36/37/38-34
WGK Germany3

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

合成工艺路线路线简述

合成目标产物 2,4,6-Trimethoxybenzaldehyde 主要起始原料 2,4,6-Trimethoxybenzyl Alcohol
621-23-8 + 1535-67-7 = 830-79-5
反应条件:1.1 Catalysts: Tin Tetrachloride Solvents: Dichloromethane; 2 H,Rt1.2 Reagents: 1-Hydroxy-1,2-Benziodoxol-3(1H)-One 1-Oxide Solvents: Dimethyl Sulfoxide,Water; 2 H,Rt1.3 Reagents: Sodium Thiosulfate Solvents: Water; Rt1.4 Reagents: Sodium Bicarbonate Solvents: Water; Basified,Rt
标题:Electrophilic Aromatic Formylation With Difluoro(Phenylsulfanyl) Methane
作者:Betterley,Nolan M.; Et Al
参考文献:Synthesis 日期:2018 卷标:50(10) 页码:2033-2040]

621-23-8 + 1535-67-7 = 830-79-5
反应条件:1.1 Catalysts: Bismuth Triflate Solvents: 1,1,1,3,3,3-Hexafluoro-2-Propanol; 5 Min,Rt1.2 Solvents: 1,1,1,3,3,3-Hexafluoro-2-Propanol; 12 H,Rt1.3 Reagents: 2-Iodoxybenzoic Acid Solvents: Dimethyl Sulfoxide,Water; 1 H,Rt1.4 Reagents: Sodium Sulfite Solvents: Water; Rt1.5 Reagents: Sodium Bicarbonate Solvents: Water; Basified,Rt
标题:Bi(Otf)3 Enabled C-F Bond Cleavage In Hfip: Electrophilic Aromatic Formylation With Difluoro(Phenylsulfanyl)Methane
作者:Betterley,Nolan M.; Et Al
参考文献:Asian Journal Of Organic Chemistry 日期:2018 卷标:7(8) 页码:1642-1647]

61040-78-6 = 830-79-5
反应条件:1.1 Reagents: Oxygen,Abts Catalysts: Laccase Solvents: Water
标题:Comparing The Catalytic Efficiency Of Some Mediators Of Laccase
作者:Fabbrini,Maura; Et Al
参考文献:Journal Of Molecular Catalysis B: Enzymatic 日期:2002 卷标:16(5-6) 页码:231-240]

61040-78-6 = 830-79-5
反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Palladium Solvents: Toluene; 90 °C
标题:Highly Dispersed Palladium Nanoparticles Supported On An Imidazolium-Based Ionic Liquid Polymer: An Efficient Catalyst For Oxidation Of Alcohols
作者:Karimi,Z.; Et Al
参考文献:Russian Chemical Bulletin 日期:2022 卷标:71(6) 页码:1194-1203]

621-23-8 + 4885-02-3 = 830-79-5
反应条件:1.1 Reagents: Titanium Tetrachloride Solvents: Dichloromethane; 0 °C; 1 H1.2 45 Min1.3 Reagents: Ammonium Chloride Solvents: Water; 2 H
标题:Formylation Of Electron-Rich Aromatic Rings Mediated By Dichloromethyl Methyl Ether And Ticl4: Scope And Limitations
作者:Ramos-Tomillero,Ivan; Et Al
参考文献:Molecules 日期:2015 卷标:20(4) 页码:5409-5422]

621-23-8 = 830-79-5
反应条件:1.1 Reagents: Boron Trifluoride Etherate,Triethyl Orthoformate Solvents: Dichloromethane1.2 Reagents: Water
标题:First Reactions Of Dialkoxycarbenium Tetrafluoroborates With Pyrroles,5H-Dibenz[b,F]Azepines,And Electron-Rich Arenes
作者:Pindur,U.; Et Al
参考文献:Journal Of Heterocyclic Chemistry 日期:1989 卷标:26(6) 页码:1563-8]

62778-01-2 = 830-79-5
反应条件:1.1 Reagents: Triethylamine Catalysts: Triphenylphosphine Solvents: Dmso-D6; Rt -> 120 °C; 12 H,120 °C
标题:Triphenylphosphine/triethylamine-Mediated Decarboxylation Of α-Oxocarboxylic Acids And Application In A One-Pot Synthesis Of Deuterated Aldehydes.
作者:Niu,Guang-Hao; Et Al
参考文献:Asian Journal Of Organic Chemistry 日期:2016 卷标:5(1) 页码:57-61]

= 830-79-5
反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone; 6 H,Rt -> Reflux2.1 Reagents: Phosphorus Oxychloride; 15 - 20 Min,0 °C; 1 H,Rt2.2 Reagents: Potassium Hydroxide Solvents: Water; Basified,0 °C
标题:Synthesis Of Structurally Diverse Biflavonoids
作者:Sum,Tze Jing; Et Al
参考文献:Tetrahedron 日期:2018 卷标:74(38) 页码:5089-5101]

= 830-79-5
反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone; 8 H,60 - 70 °C2.1 Reagents: Phosphorus Oxychloride; 0 °C; 1 H,Rt2.2 Reagents: Potassium Hydroxide Solvents: Water; Basified,Cooled
标题:Synthesis Of New C-Dimethylated Chalcones As Potent Antitubercular Agents
作者:Anandam,Rambabu; Et Al
参考文献:Medicinal Chemistry Research 日期:2018 卷标:27(6) 页码:1690-1704]

63665-97-4 = 830-79-5
反应条件:1.1 -2.1 Reagents: Phosphorus Oxychloride
标题:The Vilsmeier Reaction Of Fully Conjugated Carbocycles And Heterocycles
作者:Jones,Gurnos; Et Al
参考文献:Organic Reactions (Hoboken 日期:1997 卷标:49]

621-23-8 = 830-79-5 + 2510-49-8
反应条件:1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran,Hexane; 0 °C; 2 H,0 °C1.2 0 °C; 2 H,Rt1.3 Solvents: Methanol; 30 Min,Rt1.4 Reagents: Potassium Carbonate,Iodine; 0 °C; 41 H,Rt1.5 Reagents: Sodium Sulfite Solvents: Water; Rt
标题:Facile Preparation Of Aromatic Esters From Aromatic Bromides With Ethyl Formate Or Dmf And Molecular Iodine Via Aryllithium
作者:Ushijima,Sousuke; Et Al
参考文献:Tetrahedron 日期:2012 卷标:68(24) 页码:4701-4709]

621-23-8 = 830-79-5
反应条件:1.1 Reagents: Phosphorus Oxychloride Solvents: Dimethylformamide; 45 Min,0 °C; 1 H,0 °C1.2 Reagents: Potassium Carbonate Solvents: Water; Ph 9 - 10
标题:Enantioselective Ring Opening Of Meso-Epoxides With Silicon Tetrachloride Catalyzed By Pyridine N-Oxides Fused With The Bicyclo[3.3.1]Nonane Framework
作者:Neniskis,Algirdas; Et Al
参考文献:European Journal Of Organic Chemistry 日期:2015 卷标:2015(28) 页码:6359-6369]

949593-49-1 = 830-79-5
反应条件:1.1 Reagents: Phosphorus Oxychloride; 0 °C; 1 H,Rt1.2 Reagents: Potassium Hydroxide Solvents: Water; Basified,Cooled
标题:Synthesis Of New C-Dimethylated Chalcones As Potent Antitubercular Agents
作者:Anandam,Rambabu; Et Al
参考文献:Medicinal Chemistry Research 日期:2018 卷标:27(6) 页码:1690-1704]

621-23-8 + 93-61-8 = 830-79-5
反应条件:1.1 Reagents: Phosphorus Oxychloride; 5 - 10 Min,40 - 50 °C1.2 15 Min,70 °C1.3 Solvents: Water; 1 H,Cooled
标题:Sulfur-Substituted α-Alkyl Phenethylamines As Selective And Reversible Mao-A Inhibitors: Biological Activities,Comfa Analysis,And Active Site Modeling
作者:Gallardo-Godoy,Alejandra; Et Al
参考文献:Journal Of Medicinal Chemistry 日期:2005 卷标:48(7) 页码:2407-2419]

621-23-8 + 93-61-8 = 830-79-5
反应条件:1.1 Reagents: Phosphorus Oxychloride Solvents: Diethyl Ether
标题:Alkyl-Oxygen Fission In Carboxylic Esters. Xi. Reactions Of Secondary Alcohols Containing The 2,4,6-Trimethoxyphenyl Radical
作者:Kenyon,J.; Et Al
参考文献:Journal Of The Chemical Society 日期:1952 卷标:4964 页码:4964-9]

621-23-8 = 830-79-5
反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Benzene
标题:Mescaline Analogs. I. 2,4,6-Trialkoxyphenethylmines
作者:Benington,F.; Et Al
参考文献:Journal Of Organic Chemistry 日期:1954 卷标:19 页码:11-16]

40243-91-2 = 830-79-5
反应条件:1.1 Reagents: Hydrogen Peroxide Catalysts: Vanadium Oxide (V2O5) (Supported On Tio2) Solvents: Acetonitrile; 4 H,30 °C
标题:V2O5@tio2 Catalyzed Green And Selective Oxidation Of Alcohols,Alkylbenzenes And Styrenes To Carbonyls
作者:Upadhyay,Rahul; Et Al
参考文献:Chemcatchem 日期:2021 卷标:13(16) 页码:3594-3600]

61040-78-6 = 830-79-5
反应条件:1.1 Reagents: Potassium Carbonate,Oxygen Catalysts: Palladium Solvents: Toluene; 11 H,90 °C
标题:Palladium Pincer Complex Incorporation Onto The Fe3O4-Entrapped Crosslinked Multilayered Polymer As A High Loaded Nanocatalyst For Oxidation
作者:Zohreh,Nasrin; Et Al
参考文献:Journal Of Molecular Liquids 日期:2018 卷标:266 页码:393-404]

= 830-79-5 [标题:Reaction Conditions
标题:Photosensitized Electron-Transfer Reaction Of 3-Aryl-2-Methyloxaziridine: Direct Deoxygenation From The Isomeric Arylnitrone
作者:Iwano,Yasunori; Et Al
参考文献:Bulletin Of The Chemical Society Of Japan 日期:1994 卷标:67(8) 页码:2348-50]

= 830-79-5
反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone2.1 Reagents: Phosphorus Oxychloride Solvents: Dimethylformamide
标题:New Convenient Synthesis Of 8-C-Methylated Homoisoflavones And Analysis Of Their Structure By Nmr And Tandem Mass Spectrometry
作者:Yadav,Santosh Kumar
参考文献:International Journal Of Organic Chemistry 日期:2021 卷标:11(1) 页码:46-54]

224156-28-9 = 830-79-5
反应条件:1.1 -2.1 Reagents: Phosphorus Oxychloride
标题:The Vilsmeier Reaction Of Fully Conjugated Carbocycles And Heterocycles
作者:Jones,Gurnos; Et Al
参考文献:Organic Reactions (Hoboken 日期:1997 卷标:49]

570-02-5 = 830-79-5
反应条件:1.1 Reagents: Thionyl Chloride; 4 H,Reflux1.2 2 H,Reflux2.1 Reagents: Phosphorus Oxychloride; Cooled; 3 H,Rt2.2 Reagents: Sodium Hydroxide Solvents: Water; Overnight,Neutralized
标题:Synthesis Of Stable Free Radicals As Potential Organic Metals. Synthesis Of Oxygenated Indacene Derivatives. Reactions Of Aromatic Poly(N,N-Dimethylamides) With Electrophiles
作者:Armstrong,Mark Wayne
参考文献:1983]

44205-36-9 = 830-79-5
反应条件:1.1 -2.1 -3.1 Reagents: Phosphorus Oxychloride
标题:The Vilsmeier Reaction Of Fully Conjugated Carbocycles And Heterocycles
作者:Jones,Gurnos; Et Al
参考文献:Organic Reactions (Hoboken 日期:1997 卷标:49]

621-23-8 + 4885-02-3 = 830-79-5 + 591228-81-8
反应条件:1.1 Catalysts: Silver Triflate Solvents: Dichloromethane; -78 °C; 15 Min,0 °C1.2 Reagents: Sodium Bicarbonate Solvents: Water; 30 Min,Rt
标题:A Direct And Mild Formylation Method For Substituted Benzenes Utilizing Dichloromethyl Methyl Ether-Silver Trifluoromethanesulfonate
作者:Ohsawa,Kosuke; Et Al
参考文献:Journal Of Organic Chemistry 日期:2013 卷标:78(7) 页码:3438-3444]

32316-92-0 = 830-79-5 + 13250-06-1
反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Iridium(1+),[4,4′-Bis(1,1-Dimethylethyl)-2,2′-Bipyridine-κn1,κn1′]Bis[3,5-Diflu... Solvents: Dichloromethane; 12 H,40 °C
标题:Visible-Light-Mediated Late-Stage Sulfonylation Of Boronic Acids Via N-S Bond Activation Of Sulfonamides
作者:Zhen,Jingsong; Et Al
参考文献:Acs Catalysis 日期:2022 卷标:12(3) 页码:1986-1991

2,4,6-三甲氧基苯乙醇置于laccase,2,2,6,6-四甲基哌啶氧化物,Sodium Acetate体系中,用乙醚作为反应溶剂,以83 %的收率获得产物2,4,6-三甲氧基苯甲醛
参考文献:白腐蘑菇 Tricholoma Giganteum Aghp 漆酶选择性氧化苯甲醇:Taccabulin A,Taccabulin D 和 Taccabulin E 的全合成
标题:白腐蘑菇 Tricholoma Giganteum Aghp 漆酶选择性氧化苯甲醇:Taccabulin A,Taccabulin D 和 Taccabulin E 的全合成
摘要:使用漆酶将苄醇绿色选择性氧化为相应的醛,由蘑菇tricholoma Giganteum Aghp置于tempo 存在下作为介质在温和和环境友好的反应条件下产生,在 8-24 小时内具有优异的产率(高达 95%).这种方法的适用性已扩展到各种底物和抗癌剂,天然二氢查耳酮 Taccabulin A,Taccabulin D 和 Taccabulin E 的全合成.
DOI:10.1016/j.Tet.2022.133114

海关参考信息

2905110000-甲醇
2907221000-对苯二酚
2912110000-甲醛
2912210000-苯甲醛
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详情请参考：📖 海关编码查询和海关进出口税则

专利信息

专利号:US-7951961-B2
优先权日:2006-07-07
标题:Enantioselective synthesis of pyrrolidines substituted with flavones, and intermediates thereof
发明人：SIVAKUMAR MEENAKSHI; SHUKLA MANOJ; JADHAV PRAMOD KUMAR; BORHADE AJIT
权利人:PIRAMAL LIFE SCIENCES LTD
摘要:The present invention relates to an enantioselective synthesis of (+)-trans enantiomer of pyrrolidines substituted with flavones, represented by Formula 1 or salts thereof, which are inhibitors of cyclin dependant kinases and can be used for treatment of proliferative disorders such as cancer n nwherein Ar has the meaning as indicated in the claims.

专利号:US-9475814-B2
优先权日:2011-10-03
标题:Chiral N-acyl-5,6,7(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof
发明人：HOVEYDA HAMID R; DUTHEUIL GUILLAUME; FRASER GRAEME L; ROY MARIE-ODILE; EL BOUSMAQUI MOHAMED; BATT FREDERIC
权利人:EUROSCREEN SA
摘要:The present invention relates to novel compounds of Formula I and their use in therapeutic treatments. The invention further relates to a novel chiral synthesis of 5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines using N-sp3 protective groups. The invention also provides intermediates for use in the synthesis of compounds of Formula I.

专利号:US-8710268-B2
优先权日:2007-07-31
标题:Method for the hydrolysis of substituted formylamines into substituted amines
发明人：BOBYLEV MIKHAIL
权利人:BOBYLEV MIKHAIL
摘要:An improved method for the synthesis of substituted formylamines and substituted amines via an accelerated Leuckart reaction. The Leuckart reaction is accelerated by reacting formamide or N-alkylformamide and formic acid with an aldehyde or a ketone at a preferred molar ratio that accelerates the reaction. The improved method is applicable to various substituted aldehydes and ketones, including substituted benzaldehydes. An accelerated method for the hydrolysis of substituted formylamines into substituted amines using acid or base and a solvent at an elevated temperature. The improved method is useful for the accelerated synthesis of agrochemicals and pharmaceuticals such as vanillylamine, amphetamine and its analogs, and formamide fungicides.

专利号:US-8202985-B2
优先权日:2005-10-31
标题:Monomer compositions for the synthesis of polynucleotides, methods of synthesis, and methods of deprotection
发明人：DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINO; CARUTHERS MARVIN H
权利人:DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINO; CARUTHERS MARVIN H; AGILENT TECHNOLOGIES INC; UNIV COLORADO
摘要:Nucleotide monomers, polynucleotides, methods of making each, and methods of deprotecting each, are disclosed. An embodiment of the nucleotide monomer, among others, includes a nucleotide monomer having a heterobase protecting group selected from structures I through III as described herein. An embodiment of the polynucleotide, among others, includes a plurality of nucleotide moieties having a heterobase protecting group selected from one of structures I through III as described herein.

专利号:US-7759471-B2
优先权日:2005-10-31
标题 :Monomer compositions for the synthesis of RNA, methods of synthesis, and methods of deprotection
发明人：DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINE; CARUTHERS MARVIN H
权利人:AGILENT TECHNOLOGIES INC; UNIV COLORADO
摘要:Nucleotide monomers, polynucleotides, methods of making each, methods of deprotecting each, and the like are disclosed herein.

专利号:US-2003203915-A1
优先权日:2002-04-05
标题 :Nitric oxide donors, compositions and methods of use related applications
发明人：FANG XINQIN; GARVEY DAVID S; GASTON RICKY D; LIN CHIA-EN; RANATUNGA RAMANI R; RICHARDSON STEWART K; WANG TIANSHENG; WANG WEIHENG; WEY SHIOW-JYI
权利人:FANG XINQIN; GARVEY DAVID S; GASTON RICKY D; LIN CHIA-EN; RANATUNGA RAMANI R; RICHARDSON STEWART K; WANG TIANSHENG; WANG WEIHENG; WEY SHIOW-JYI
摘要:The invention describes novel nitric oxide donors and novel compositions comprising at least one nitric oxide donor. The invention also provides novel compositions comprising at least one nitric oxide donor, and, optionally, at least one therapeutic agent. The compounds and compositions of the invention can also be bound to a matrix. The invention also provides methods for treating cardiovascular diseases, for the inhibition of platelet aggregation and platelet adhesion caused by the exposure of blood to a medical device, for treating pathological conditions resulting from abnormal cell proliferation; transplantation rejections, autoimmune, inflammatory, proliferative, hyperproliferative, vascular diseases; for reducing scar tissue or for inhibiting wound contraction, particularly the prophylactic and/or therapeutic treatment of restenosis by administering the nitric oxide donor optionally in combination with at least one therapeutic agent. The invention also provides methods for treating inflammation, pain, fever, gastrointestinal disorders, respiratory disorders and sexual dysfunctions. The nitric oxide donors donate, transfer or release nitric oxide, and/or elevate endogenous levels of endothelium-derived relaxing factor, and/or stimulate endogenous synthesis of nitric oxide and/or are substrates for nitric oxide synthase and are capable of releasing nitric oxide or indirectly delivering or transferring nitric oxide to targeted sites under physiological conditions. The therapeutic agent can optionally be substituted with at least one NO and/or NO 2 group (i.e., nitrosylated and/or nitrosated). The invention also provides novel compositions and kits comprising at least one nitric oxide donor and/or at least one therapeutic agent.

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2,4,6-三甲氧基苯甲醛

2,4,6-Trimethoxybenzaldehyde

纯度:98
250kg/drum

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主要参考文献

参考标题:Construction Of 2-Substituted-3-Functionalized Benzofurans Via Intramolecular Heck Coupling: Application To Enantioselective Total Synthesis Of Daphnodorin B
作者:Hu Yuan,Kai-Jian Bi,Bo Li,Rong-Cai Yue,Ji Ye,Yun-Heng Shen,Lei Shan,Hui-Zi Jin,Qing-Yan Sun,Wei-Dong Zhang |发布日期:2013.9.20
摘要:A Novel Approach Was Developed For The Synthesis Of 2-Substituted-3-Functionalized Benzofurans, Using An Intramolecular Heck Reaction Which Was Further Applied In The First Enantioselective Total Synthesis Of Daphnodorin B.

合成参考文献

摘要:Minbiole, K. P. C., Science of Synthesis, (2009) 46, 166.
摘要:Beier, P., Science of Synthesis Knowledge Updates, (2014) 2, 320.
摘要:Tsubouchi, A., Science of Synthesis Knowledge Updates, (2016) 2, 329.
摘要:Leung, M.-k.; Chou, C.-M.; Luh, T.-Y., Science of Synthesis Knowledge Updates, (2018) 2, 420.
摘要:Tsubouchi, A., Science of Synthesis Knowledge Updates, (2016) 2, 335.

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CAS: 830-79-5; 2,4,6-Trimethoxybenzaldehyde

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