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Cyclohexanone, 2-(2-chloroethyl)-, also known as 2-(2-chloroethyl)cyclohexanone or chloroethyl cyclohexyl ketone, is an organic compound with the chemical formula C8H13ClO. It is a colorless to pale yellow liquid with a molecular weight of 156.65 g/mol. Cyclohexanone, 2-(2-chloroethyl)- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a chemical warfare agent due to its cytotoxic properties. Cyclohexanone, 2-(2-chloroethyl)-, is a hazardous substance and requires proper handling and disposal to minimize environmental and health risks.

2402-57-5

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2402-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2402-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2402-57:
(6*2)+(5*4)+(4*0)+(3*2)+(2*5)+(1*7)=55
55 % 10 = 5
So 2402-57-5 is a valid CAS Registry Number.

2402-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloroethyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,2-(2-chloroethyl)

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:2402-57-5 SDS

2402-57-5Relevant academic research and scientific papers

N-dihydroxyalkyl-substituted 2-oxo-imidazole derivatives

-

Page/Page column 10, (2010/11/25)

The invention provides the compounds represented by the formula (I) in which, R stands for a dihydroxy-substituted C1-C6 alkyl group, and Cy stands for an optionally substituted C6-C10 bi- or tri-cyclic aliphati

Synthesis and Thermolysis of O-Alkyl-N-vinylhydroxylamine Derivatives

Shatzmiller, Shimon,Shalom, Eytan

, p. 897 - 905 (2007/10/02)

Oxoiminium salts 11 a-e and 13 a-e have been prepared from the ο-chloroketones 9 a-e by oximation via the cyclic oxime ethers 10 a-e and the cyclic imine oxides 12 a-e, followed by alkylation with "Meerwein salt".The deprotonation reaction of 11 a-e and 13 a-e yields, via the regioselectively prepared intermediates 14 a-e and 17 a-e, the α, β-unsaturated imines 15 a-e and the cyclic imines 18 a-e, respectively.

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