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2H-Azepin-2-one, hexahydro-1-(1-oxopentyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7564-42-3

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7564-42-3 Usage

Classification

Heterocyclic compound

Class

Azepines

Ring size

Six-membered

Functional groups

Ketone group, pentyl side chain

Applications

Organic synthesis, pharmaceutical industry

Pharmacological activities

Potential

Uses

Synthesis of drugs, bioactive compounds

Check Digit Verification of cas no

The CAS Registry Mumber 7564-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7564-42:
(6*7)+(5*5)+(4*6)+(3*4)+(2*4)+(1*2)=113
113 % 10 = 3
So 7564-42-3 is a valid CAS Registry Number.

7564-42-3SDS

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-pentanoylazepan-2-one

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:7564-42-3 SDS

7564-42-3Downstream Products

7564-42-3Relevant academic research and scientific papers

Practical and General Manganese-Catalyzed Carbonylative Coupling of Alkyl Iodides with Amides

Li, Yahui,Zhu, Fengxiang,Wang, Zechao,Rabeah, Jabor,Brückner, Angelika,Wu, Xiao-Feng

, p. 915 - 919 (2017)

A selective manganese-catalyzed carbonylative transformation of alkyl iodides and amides was developed. A variety of imides were prepared in moderate to good yields. Alkyl bromides could also be applied by in situ treatment with NaI to give the corresponding alkyl iodides. Notably, no additives or expensive ligands were required here. As the first example of the carbonylative coupling of alkyl iodides with amides, the simple reaction conditions and the advantages of a manganese catalyst make this new general procedure more attractive and practical than conventional techniques. Mechanistically, control experiments and electron paramagnetic resonance spectroscopy studies were also performed, and the radical nature of this new process was proven.

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