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Merck

640573

Sigma-Aldrich

环丙磺酰氯

95%

别名:

Cyclopropylsulfonyl chloride

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About This Item

经验公式(希尔记法):
C3H5ClO2S
分子量:
140.59
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

95%

折射率

n20/D 1.4770 (lit.)

密度

1.38 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

ClS(=O)(=O)C1CC1

InChI

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

InChI 密鑰

PFWWSGFPICCWGU-UHFFFAOYSA-N

應用

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.

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

204.8 °F - closed cup

閃點(°C)

96 °C - closed cup

個人防護裝備

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


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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)

商品

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

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

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

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

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