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M7707

2-Mesitylenesulfonyl chloride

99%

Synonym(s):

2,4,6-Trimethylbenzenesulfonyl chloride

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$338.00

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About This Item

Linear Formula:
(CH3)3C6H2SO2Cl
CAS Number:
773-64-8
Molecular Weight:
218.70
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897176
EC Number:
212-257-8
Beilstein/REAXYS Number:
1107601
MDL number:
MFCD00007434
Assay:
99%
Form:
crystals

Key Documents

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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

200

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This Item
129631119490C95501
2-Mesitylenesulfonyl chloride 99%

Sigma-Aldrich

M7707

2-Mesitylenesulfonyl chloride

2-Mesitylenesulfonic acid dihydrate 97%

Sigma-Aldrich

129631

2-Mesitylenesulfonic acid dihydrate

2,4,6-Triisopropylbenzenesulfonyl chloride 97%

Sigma-Aldrich

119490

2,4,6-Triisopropylbenzenesulfonyl chloride

Cyanuric chloride 99%

Sigma-Aldrich

C95501

Cyanuric chloride

assay

99%

assay

97%

assay

97%

assay

99%

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200

form

crystals

form

solid

form

solid

form

powder

mp

55-57 °C (lit.)

mp

74-78 °C (lit.)

mp

92-94 °C (lit.)

mp

145-147 °C (lit.)

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

signalword

Danger

hcodes

H314

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8577
BCCD1020
BCBW6161
BCBW0403
BCBV2770

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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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