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Merck
CN

640573

Cyclopropanesulfonyl chloride

95%

Synonym(s):

Cyclopropylsulfonyl chloride

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About This Item

Empirical Formula (Hill Notation):
C3H5ClO2S
CAS Number:
Molecular Weight:
140.59
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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Product Name

Cyclopropanesulfonyl chloride, 95%

InChI

1S/C3H5ClO2S/c4-7(5,6)3-1-2-3/h3H,1-2H2

SMILES string

ClS(=O)(=O)C1CC1

InChI key

PFWWSGFPICCWGU-UHFFFAOYSA-N

assay

95%

refractive index

n20/D 1.4770 (lit.)

density

1.38 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

Related Categories

Application

Cyclopropanesulfonyl chloride can be used in the synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic sulfonamide derivatives, which can serve as building blocks in the preparation of potent hepatitis C virus NS3 protease inhibitors.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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"Concise asymmetric synthesis of a (1R, 2S)-1-amino-2-vinylcyclopropanecarboxylic acid-derived sulfonamide and ethyl ester"
Lou Sha, et al.
Organic & Biomolecular Chemistry, 11(39), 6796-6805 (2013)

Articles

Sulfonyl chlorides are often chosen as building blocks in medicinal chemistry for their ability to easily react with heterocyclic amines to create complex sulfonamides.

磺酰氯通常被选用为药物化学中的结构单元,因为它们能够容易地与杂环胺反应而产生复合磺酰胺。

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