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2H-Azepin-2-one, 1,3,4,5-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2228-76-4

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2228-76-4 Usage

Main properties

Molecular formula: C6H9NO
Heterocyclic organic compound
Seven-membered ring containing one nitrogen atom and one oxygen atom

Specific content

Commonly used as a substrate in organic synthesis and pharmaceutical research
Exhibits antifungal, antibacterial, and antiviral properties
Investigated for potential as a building block in the development of new drug molecules
Valuable chemical in medicinal chemistry for its versatile reactivity and pharmaceutical potential

Check Digit Verification of cas no

The CAS Registry Mumber 2228-76-4 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 2228-76:
(6*2)+(5*2)+(4*2)+(3*8)+(2*7)+(1*6)=74
74 % 10 = 4
So 2228-76-4 is a valid CAS Registry Number.

2228-76-4SDS

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 1,3,4,5-tetrahydroazepin-2-one

1.2 Other means of identification

Product number -
Other names 2H-Azepin-2-one,1,3,4,5-tetrahydro

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:2228-76-4 SDS

2228-76-4Downstream Products

2228-76-4Relevant academic research and scientific papers

Process for producing epsilon-caprolactam

-

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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