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2228-79-7

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2228-79-7 Usage

Chemical Structure

Cyclic structure containing nitrogen and oxygen atoms

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Therapeutic Applications

a. GABAA receptor modulator
b. Potential treatment for anxiety and neurological disorders

Building Block

Used in the preparation of heterocyclic compounds

Antimicrobial Properties

Investigated for its antimicrobial properties

Versatility

Range of potential applications in pharmaceuticals, agrochemicals, and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 2228-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2228-79:
(6*2)+(5*2)+(4*2)+(3*8)+(2*7)+(1*9)=77
77 % 10 = 7
So 2228-79-7 is a valid CAS Registry Number.

2228-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydroazepin-7-one

1.2 Other means of identification

Product number -
Other names 1,5,6,7-Tetrahydro-2H-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2228-79-7 SDS

2228-79-7Relevant articles and documents

Process for producing epsilon-caprolactam

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Paragraph [0056] - [0059], (2008/06/13)

A high purity ε-caprolactam is prepared by pouring a molten crude ε-caprolactam and a solvent comprising an aliphatic hydrocarbon and having a lower temperature than that of the crude ε-caprolactam, into a vessel and mixing them to obtain a first slurry containing a crystallized ε-caprolactam. The slurry is then subjected to a solid-liquid separation to obtain ε-caprolactam and a first liquid phase. This process can effectively remove impurities from a crude ε-caprolactam, which is obtained by for example, subjecting cyclohexanone oxime to the Beckmann rearrangement.

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