CAS: 642-31-9; 9-Anthraldehyde

该化合物是属于甲醚类的有机化合物,其特点是炭疽脊椎,这是一种多环芳烃,附着于9位置的气态组(CHO),其特征是室内温度的固态,通常表现为黄色和浅褐色晶体物质,其熔点相对高,在水中溶解,但在乙醇和二氯甲烷等有机溶剂中较易溶解. 9-苯甲酸酯因其在有机合成中的应用而已知,特别是在各种衍生物的制作过程中,以及作为开发荧光材料和染料的建筑块.此外,该化合物具有有趣的光物理特性,有助于与光化装置有关的研究.与许多芳香的甲醚一样,如果吸入或吸入,则可能对健康造成危害,因此需要在处理过程中采取适当的安全措施.

结构式图片

相似化合物

1210-12-4 723-62-6 34810-13-4

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

chloromethylene-formamidine anthracene N,N-dimethyl-formamide N-methyl-N-phenylformamide (E)-3-(anthracen-9-yl)acrylic acid (Z)-3-(anthracen-9-yl)-2-phenylacrylonitrile (E)-3-(anthracen-9-yl)-1-(2-hydroxyphenyl)prop-2-en-3-one [9]anthryl-benzoyloxy-acetonitrile

合成工艺路线路线简述

  • 合成目标产物 9-Anthraldehyde 主要起始原料 1,1-Dichlorodimethyl Ether And Anthracene
  • (文献来源)合成步骤主要原料 1,1-Dichlorodimethyl Ether 和 Anthracene
1-Anthracen-9-Yl-N-Tert-Butylmethanimine置于水体系中,化学反应生成 9-蒽甲醛
参考文献:由芳基卤和醛的钯催化合成的叔丁基胩使用甲酸盐作为氢化物供体†
标题:由芳基卤和醛的钯催化合成的叔丁基胩使用甲酸盐作为氢化物供体†
摘要:通过使用叔丁基异氰化物作为c 1资源和甲酸盐作为氢化物供体,无需任何其他碱,就已经实现了芳烃卤化物的高效一锅钯催化的芳基卤化物的加氢甲酰化反应.反应条件温和,易于操作且毒性较低,该反应可耐受各种官能团,产率中等至优异.
DOI:10.1039/c4Ra16388E

海关参考信息

专利信息


专利号:US-2008146772-A1
优先权日:2006-11-02
标题 :Materials and methods for co-crystal controlled solid-state synthesis of imides and imines
发明人:ZAWOROTKO MICHAEL J; CHENEY MIRANDA L
权利人:UNIV SOUTH FLORIDA
摘要:The subject invention pertains to methods for solid-state synthesis of imides and imines using co-crystals. The co-crystal formers utilized are substrates of condensation reactions and co-crystals can be obtained in high yield via methods such as slurrying, solvent evaporation, solvent crystallization, treatment with supercritical fluid(s), melting plus crystallization, slurry conversion, grinding of solids, blending of powders, heating of solids, solvent-drop grinding, or grinding plus melting.

专利号:US-6417380-B1
优先权日:1987-12-31
标 题 :Synthesis of 1,2-dioxetanes and intermediates therefor
发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
摘要:Compounds having the formula: n wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., n m-phenylene), produced by reacting a compound having the formula: n with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: n are produced by reacting a compound having the formula: n with n wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula n are produced by reacting a compound of the formula n with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

专利号:US-5777133-A
优先权日:1987-12-31
标 题:Synthesis of 1, 2-dioxetanes and intermediates therefor
发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
权利人:TROPIX INC
摘要:Compounds having the formula: ##STR1## wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (eg., m-phenylene), produced by reacting a compound having the formula: ##STR2## with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: ##STR3## are produced by reacting a compound having the formula: ##STR4## wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula ##STR5## are produced by reacting a compound of the formula ##STR6## with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

专利号:US-4956477-A
优先权日:1987-12-31
标 题:Synthesis of 1,2-dioxetanes
发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
权利人:TROPIX INC
摘要:Compounds having the formula: ##STR1## wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., m-phenylene), produced by reacting a compound having the formula: ##STR2## with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: ##STR3## are produced by reacting a compound having the formula: ##STR4## wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula ##STR5## are produced by reacting a compound of the formula ##STR6## with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

专利号:US-6916982-B2
优先权日:2000-07-21
标题:Synthesis of perylene-porphyrin building blocks and polymers thereof for the production of light-harvesting arrays
发明人:LOEWE ROBERT S; TOMIZAKI KIN-YA; LINDSEY JONATHAN S
权利人:UNIV NORTH CAROLINA STATE
摘要:The present invention provides methods, compounds, and compositions for the synthesis of light harvesting arrays, such arrays comprising: (a) a first substrate comprising a first electrode; and (b) a layer of light harvesting rods electrically coupled to said first electrode, each of said light harvesting rods comprising a polymer of Formula I:n nX 1 X m+1 ) m   (I)n nwherein m is at least 1; X 1 is a charge separation group, and X 2 through X m+1 are chromophores. At least one of X 2 through X m+1 has at least one perylene group coupled thereto.

专利号:US-2022356139-A1
优先权日:2019-09-03
标 题:Synthesis of deuterated aldehydes
发明人:WANG WEI
权利人:ARIZONA BOARD OF REGENTS ON BEHALF OF ATHE UNIV OF ARIZONA
摘要:Described are methods for preparing a deuterated aldehyde using N-heterocyclic carbene catalysts in a solvent comprising D 2 O. The methods may be used to convert a wide variety of aldehydes (e.g., aryl, alkyl, or alkenyl aldehydes) to C-1 deuterated aldehydes under mild reaction conditions without functionality manipulation.
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主要参考文献

参考标题:Synthesis Of 1,3-Diaryl Benzo[c]Thiophenes
作者:Arasambattu K. Mohanakrishnan,P. Amaladass |发布日期:2005.6
摘要:An Array Of 1,3-Diarylbenzo[c]Thiophenes Has Been Synthesized Via The Ring Opening Of Lactones Followed By Thionation Using Lawesson'S Reagent.

合成参考文献


参考文献:10.1107/s1600536811016837
摘要:Han JR, Wang W, Zhen XL, Tian X, Liu SX. (Anthracen-9-ylmeth-yl)benzyl-ammonium chloride. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67(Pt 6):o1482.
参考文献:10.1021/tx200080b
摘要:Amunom I, Dieter LJ, Tamasi V, Cai J, Conklin DJ, Srivastava S, Martin MV, Guengerich FP, Prough RA. Cytochromes P450 catalyze the reduction of α,β-unsaturated aldehydes. Chem Res Toxicol. 2011 Aug 15;24(8):1223–30.
参考文献:10.3724/sp.j.1123.2011.00368
摘要:Jin J, Huang H, Lee W. [Enantiomer separation of alpha-amino acid methyl esters and some aliphatic amines as 9-anthraldimine derivatives by high performance liquid chromatography]. Se Pu. 2011 Apr;29(4):368–72. doi: 10.3724/sp.j.1123.2011.00368.
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