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M7707

Sigma-Aldrich

均三甲苯基磺酰氯

99%

别名:

2,4,6-三甲基苯磺酰氯

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5 G
$41.70
25 G
$138.00
100 G
$390.00

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5 G
$41.70
25 G
$138.00
100 G
$390.00

About This Item

线性分子式:
(CH3)3C6H2SO2Cl
CAS号:
773-64-8
分子量:
218.70
Beilstein:
1107601
EC 号:
212-257-8
MDL编号:
MFCD00007434
UNSPSC代码:
12352100
PubChem化学物质编号:
24897176
NACRES:
NA.22

$41.70

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质量水平

200

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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相关类别

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. [1] [2]

应用

多核苷酸合成中的偶联剂。[3]

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCD1020
BCBW6161
BCBW0403
BCBV2770
BCBF9313V

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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
Tetrahedron, 48, 1729-1729 (1992)
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)
Synthesis of 28-O-(1, 2-Diacyl-SN-glycero-3-phospho)-betulin
B Tubek, et al.
Synthetic Communications, 42, 3648-3654 (2012)

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