- 英文名称4-Methoxy-2,3,6-Trimethylbenzene-1-Sulfonyl Chloride
- 中文名称4-甲氧基-2,3,6-三甲基苯磺酰氯
- IUPAC名称4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride
- 其它别名4-甲氧基-2,3,6-三甲基苯磺酰基氯; 4-Methoxy-2,3,6-Trimethylbenzenesulphonyl Chloride
- CAS编号80745-07-9
- MFCD编号:MFCD00038846
- EINECS号:626-430-4
- 分子式:C10H13ClO3S分子量:248.73
- 产品CID: 1802588
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
欧盟法规
ECHA物质C&L通报上下游产品
CAS号20469-61-8 2,3,5-三甲基苯甲醚 | CAS号697-82-5 2,3,5-三甲基苯酚 | CAS号80745-10-4 N'-(4-甲氧基-2,3,6... | CAS号80745-09-1 |N|-苄氧羰基-|N|'-(...合成工艺路线路线简述
- 697-82-5 = 80745-07-9 [标题:Reaction Conditions
标题:Protecting And Restoring Guanidino Group
参考文献:European Patent Organization]
20469-61-8 = 80745-07-9
反应条件:1.1 Reagents: Chlorosulfonic Acid Solvents: Dichloromethane; 0 °C; 1 H,0 °C
标题:Ligand-Controlled Diastereodivergency In Propargylic Alkylation Of Vinylogous Aza-Enamines: Construction Of 1,3-Stereocenters
作者:Ghosh,Suman; Et Al
参考文献:Organic Letters 日期:2023 卷标:25(40) 页码:7304-7309]
20469-61-8 = 80745-07-9
反应条件:1.1 Reagents: Chlorosulfonic Acid
标题:Histidine-Containing Peptides
参考文献:Japan]
697-82-5 = 80745-07-9
反应条件:1.1 Reagents: Sodium Hydride Solvents: Tetrahydrofuran; 0 °C; 1 H,0 °C1.2 3 H,25 °C2.1 Reagents: Chlorosulfonic Acid Solvents: Dichloromethane; 0 °C; 1 H,0 °C
标题:Ligand-Controlled Diastereodivergency In Propargylic Alkylation Of Vinylogous Aza-Enamines: Construction Of 1,3-Stereocenters
作者:Ghosh,Suman; Et Al
参考文献:Organic Letters 日期:2023 卷标:25(40) 页码:7304-7309
📜2,3,5-三甲基苯酚置于氯磺酸,Sodium Hydride体系中,用 四氢呋喃,二氯甲烷 作为反应溶剂,化学反应 5.0H,反应生成 4-甲氧基-2,3,6-三甲基苯磺酰氯
参考文献:在相转移催化的不对称strecker反应中由α-酰胺砜原位反应生成n-芳基磺酰基亚胺的优势
标题:在相转移催化的不对称strecker反应中由α-酰胺砜原位反应生成n-芳基磺酰基亚胺的优势
摘要:在甲苯-氰化钾水溶液双相条件下,使用手性季铵碘化铵(r,R,R)-1作为有效相,已经可以从相应的α-酰胺基砜高效催化对映选择性地合成n-芳基磺酰基α-氨基腈.-转移催化剂.涉及原位反应生成反应性n-磺酰基亚胺的这种strecker合成方法对于具有伯和仲烷基取代基的底物的氰化是有利的.
DOI:10.1016/j.Tetlet.2006.12.122
海关参考信息
- 2902300000-甲苯
2905110000-甲醇
2907121100-间甲酚
2908199090-其他酚的卤化衍生物 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 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-4416820-A
优先权日:1981-01-14
标题:Indole derivatives and a method for production of peptides
发明人:FUKUDA TSUNEHIKO; KOBAYASHI SHIGERU; FUJINO MASAHIKO
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:An indole group in an amino acid or a peptide can be protected with a group shown by the formula: wherein R1 and R5 each is hydrogen, methyl or methoxy; R2 and R4 each is hydrogen or methyl; and R3 is methyl or methoxy, and said group may easily be removed without affecting the amino acid or the peptide to be derived from the protected amino acid or peptide. Thus, the present invention is useful in the synthesis of a peptide containing an indole group.
专利号:US-2005239804-A1
优先权日:1999-06-30
标 题 :Method for improved chemical synthesis of guanidinium alkaloids
专利号:US-5627283-A
优先权日:1991-05-11
标题:Amidinophenylalanine derivatives, a process for the preparation thereof, use thereof and agents containing these as anticoagulants
发明人:STUEBER WERNER DR; DICKNEITE GERHARD DR; KOSCHINSKY RAINER
权利人:BEHRINGWERKE AG
摘要:Amidinophenylalanine derivatives of the formula I (I) the synthesis of these compounds, the use thereof and pharmaceutical agents which contain these compounds are described.
专利号:US-4476051-A
优先权日:1981-10-29
标 题 :Method for protecting amino group and restoring the same
发明人:FUJINO MASAHIKO; WAKIMASU MITSUHIRO
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:An ω-amino group and/or α-amino group in an amino acid or a peptide can be protected with a 4-methoxy-2,3,6-trimethylbenzenesulfonyl group, and said group may easily be removed without affecting the amino acid or the peptide. Thus, the present invention is useful in the synthesis of peptide containing ω-amino group and/or α-amino group.
专利号:US-4487726-A
优先权日:1980-02-12
标题:4-Methoxy-2,3,6-trimethylbenzenesulfonyl chloride
发明人:FUJINO MASAHIKO; NISHIMURA OSAMU
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:A guanidino group in an amino acid or a peptide can be protected with a specific group, i.e. pentamethylbenzenesulfonyl, 2,4,6-trimethoxybenzenesulfonyl, 4-methoxy-2,3,5,6-tetramethylbenzenesulfonyl, 4-methoxy-2,6-dimethylbenzenesulfonyl or 4-methoxy-2,3,6-trimethylbenzenesulfonyl, and said group may easily be removed without affecting the amino acid or the peptide to be derived from the protected amino acid or peptide. Thus, the present invention is useful in the synthesis of peptides containing the guanidino group.
专利号:RU-2088591-C1
优先权日:1991-05-11
标 题:Derivatives of amidinophenylalanine, method of their synthesis and amidinophenylalanine derivatives showing anticoagulating activity