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99372-97-1

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99372-97-1 Usage

Physical state

Yellowish liquid

Odor

Faint

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Functional groups

Contains a cyano group (–C≡N) and a cyclic ketone group

Reactions

Can undergo alkylation, acylation, and nucleophilic addition

Derivatives

Can produce substituted cyanocyclopentanones

Importance

Serves as a versatile intermediate in the production of diverse chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 99372-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,7 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99372-97:
(7*9)+(6*9)+(5*3)+(4*7)+(3*2)+(2*9)+(1*7)=191
191 % 10 = 1
So 99372-97-1 is a valid CAS Registry Number.

99372-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopentanecarbonitrile, 1-ethyl-2-oxo-

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2-oxocyclopentanecarbonitrile

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:99372-97-1 SDS

99372-97-1Relevant articles and documents

Lithium naphthalenide induced reductive alkylation of α-cyano ketones. A general method for regiocontrol of α,α-dialkylation of ketones

Liu, Hsing-Jang,Zhu, Jia-Liang,Shia, Kak-Shan

, p. 4183 - 4186 (2007/10/03)

An efficient general method for the consecutive introduction of two alkyl groups to the α carbon of a ketone carbonyl has been developed, making use of the lithium naphthalenide induced reductive alkylation of an α-cyano ketone system as a key operation.

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