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3-Chloroazepan-2-one is an organic compound with the chemical formula C7H11ClNO2. It is a derivative of azepan-2-one, featuring a seven-membered cyclic structure with a chloro substituent at the third carbon position. 3-chloroazepan-2-one is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of sedatives, tranquilizers, and other central nervous system agents. Due to its reactivity and potential applications, 3-chloroazepan-2-one is of interest in the fields of medicinal chemistry and chemical research.

1468-55-9

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1468-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1468-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1468-55:
(6*1)+(5*4)+(4*6)+(3*8)+(2*5)+(1*5)=89
89 % 10 = 9
So 1468-55-9 is a valid CAS Registry Number.

1468-55-9SDS

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 3-chloroazepan-2-one

1.2 Other means of identification

Product number -
Other names 3-chloro-hexahydro-azepin-2-one

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 -
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More Details:1468-55-9 SDS

1468-55-9Relevant academic research and scientific papers

Process for preparing α-chloro-ε-caprolactam

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, (2008/06/13)

A process is described for preparing α-chloro-ε-caprolactam, an intermediate for the synthesis of L-lysine, comprising reacting an N-substituted -α-chloro-ε-caprolactam, wherein the N-substituent is an organic radical selected from the group consisting of arylsulfonyl, aroyl and alkanoyl radicals, with ε-caprolactam at a temperature within the range of about 50° to about 250° C to form α-chloro-ε-caprolactam and an N-substituted-ε-caprolactam. A continuous process is also described for the production of α-chloro-ε-caprolactam further comprising the chlorination of N-substituted-ε-caprolactam to produce N-substituted-α-chloro-ε-caprolactam.

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