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2-Quinolineacetic acid, a-cyano-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22190-15-4

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22190-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22190-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22190-15:
(7*2)+(6*2)+(5*1)+(4*9)+(3*0)+(2*1)+(1*5)=74
74 % 10 = 4
So 22190-15-4 is a valid CAS Registry Number.

22190-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyano-2-quinolin-2-ylacetate

1.2 Other means of identification

Product number -
Other names cyano-quinolin-2-yl-acetic acid ethyl ester

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:22190-15-4 SDS

22190-15-4Downstream Products

22190-15-4Relevant academic research and scientific papers

Reaction of 2-quinolyl thiocyanate with C-nucleophiles

Iijima,Hiyoshi,Miyashita

, p. 1090 - 1093 (2007/10/02)

2-Quinolyl thiocyanate (2) was found to react with C-nucleophiles, i.e., phenylacetonitrile, p-chlorophenylacetonitrile, p-cyanophenylacetonitrile, p-methoxyphenylacetonitrile, ethyl cyanoacetate, and malononitrile, in two ways, depending on the nature of

REACTIONS OF QUINOLINE 1-OXIDE WITH CYANOACETIC ACID DERIVATIVES BEARING LEAVING GROUPS

Hamana, Masatomo,Fujimura, Yasuo,Nawata, Yoshiharu

, p. 235 - 239 (2007/10/02)

Quinoline 1-oxide reacts with bromocyanoacetic acid derivative (1a, 1b and 2a) in the presence of acetic anhydride to afford 2-substituted quinolines (3a, 3b and 6) through the vicarious nucleophilic substitution and the subsequent deoxygenation.From reac

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