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554243

3-氯-4-甲基苯磺酰氯

97%

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关于此项目

线性分子式:
ClC6H3(CH3)SO2Cl
化学文摘社编号:
42413-03-6
分子量:
225.09
NACRES:
NA.22
PubChem Substance ID:
24879385
UNSPSC Code:
12352100
EC Number:
412-890-1
MDL number:
MFCD00203987
Assay:
97%
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assay

97%

mp

34-38 °C (lit.)

SMILES string

Cc1ccc(cc1Cl)S(Cl)(=O)=O

InChI

1S/C7H6Cl2O2S/c1-5-2-3-6(4-7(5)8)12(9,10)11/h2-4H,1H3

InChI key

GNYVVCRRZRVBDD-UHFFFAOYSA-N

General description

3-Chloro-4-methylbenzenesulfonyl chloride can be prepared from 4-methylbenzenesulfonyl chloride via chlorination.

Application

3-Chloro-4-methylbenzenesulfonyl chloride may be used in the synthesis of 2-chloro 4-methylsulfonamide benzylamine.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 2

ppe

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
S82253V
S82253
02211JH
U21856
02616PE

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Steven J Taylor et al.
Bioorganic & medicinal chemistry letters, 19(20), 5864-5868 (2009-09-18)
A series of potent nicotinamide inhibitors of soluble epoxides hydrolase (sEH) is disclosed. This series was designed using structure-based deconstruction and a combination of two HTS hit series, resulting in hybrid analogs that retained the optimal potency from one series
Wiley-VCH
Ullmann's Fine Chemicals, 295-295 (2014)

全球贸易项目编号

货号GTIN
554243-1G04061825896731
554243-5G04061832419749