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4332-55-2

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4332-55-2 Usage

Type of compound

Acylamide derivative

Functional group

Chloroethylthio group attached to the carbon chain

Potential use

Alkylating agent in the synthesis of pharmaceuticals

Biological activity

Antitumor activity, potential use in cancer treatment

Research interest

Synthesis of new organic compounds with biological activity

Applications

Pharmaceutical and medicinal, due to its chemical properties and biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 4332-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4332-55:
(6*4)+(5*3)+(4*3)+(3*2)+(2*5)+(1*5)=72
72 % 10 = 2
So 4332-55-2 is a valid CAS Registry Number.

4332-55-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloroethylsulfanyl)acetamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4332-55-2 SDS

4332-55-2Downstream Products

4332-55-2Relevant articles and documents

Synthesis and antimycobacterial activity of pyridinium compounds with sulfonylacetamide substituent in N-alkyl chain

Shulaeva, Marina M.,Kravchenko, Marionella A.,Semenov, Vyacheslav E.

, p. 868 - 874 (2018/11/10)

[Figure not available: see fulltext.] Pyridines containing amine, amide, or hydrazide substituent were quaternized with (ω-haloalkyl)sulfonylacetamides, resulting in new pyridinium compounds that exhibited tuberculostatic activity against the strain H37Rv

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