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质量水平
方案
99%
表单
crystals
mp
55-57 °C (lit.)
SMILES字符串
Cc1cc(C)c(c(C)c1)S(Cl)(=O)=O
InChI
1S/C9H11ClO2S/c1-6-4-7(2)9(8(3)5-6)13(10,11)12/h4-5H,1-3H3
InChI key
PVJZBZSCGJAWNG-UHFFFAOYSA-N
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一般描述
2-Mesitylenesulfonyl chloride, also known as 2,4,6-Trimethylbenzenesulfonyl chloride, is an organic compound that is commonly used as a coupling agent in the nucleophilic substitution reaction to synthesize novel phospholipid derivatives of botulin and cyclodextrin.
应用
多核苷酸合成中的偶联剂。
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Tetrahedron, 48, 1729-1729 (1992)
Stéphane Menuel et al.
Beilstein journal of organic chemistry, 16, 2598-2606 (2020-11-03)
The mechanically assisted synthesis of organic compounds has recently focused considerable attention as it may be unique in features to selectively direct the reaction pathway. In the continuation of our work on the synthesis of modified cyclodextrins (CDs) via mechanochemical
Synthesis of 28-O-(1, 2-Diacyl-SN-glycero-3-phospho)-betulin
B Tubek, et al.
Synthetic Communications, 42, 3648-3654 (2012)
A family of single-isomer, dicationic cyclodextrin chiral selectors for capillary electrophoresis: M ono-6A-ammonium-6C-butylimidazolium-beta-cyclodextrin chlorides
Yun D, et al.
Electrophoresis, 34, 833-840 (2013)
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