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M7707

Sigma-Aldrich

2-Mesitylenesulfonyl chloride

99%

Synonym(s):

2,4,6-Trimethylbenzenesulfonyl chloride

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About This Item

Linear Formula:
(CH3)3C6H2SO2Cl
CAS Number:
773-64-8
Molecular Weight:
218.70
Beilstein:
1107601
EC Number:
212-257-8
MDL number:
MFCD00007434
UNSPSC Code:
12352100
PubChem Substance ID:
24897176
NACRES:
NA.22

Quality Level

200

Assay

99%

form

crystals

mp

55-57 °C (lit.)

SMILES string

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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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.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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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