M7707
2-Mesitylenesulfonyl chloride
99%
Synonym(s):
2,4,6-Trimethylbenzenesulfonyl chloride
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About This Item
Linear Formula:
(CH3)3C6H2SO2Cl
CAS Number:
Molecular Weight:
218.70
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-257-8
Beilstein/REAXYS Number:
1107601
MDL number:
Assay:
99%
Form:
crystals
InChI key
PVJZBZSCGJAWNG-UHFFFAOYSA-N
InChI
1S/C9H11ClO2S/c1-6-4-7(2)9(8(3)5-6)13(10,11)12/h4-5H,1-3H3
SMILES string
Cc1cc(C)c(c(C)c1)S(Cl)(=O)=O
assay
99%
form
crystals
mp
55-57 °C (lit.)
Quality Level
Related Categories
General description
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.
Application
Coupling reagent in polynucleotide synthesis.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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)
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)
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