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Ethanone, 1-(4-chlorophenyl)-2-(tetrahydro-2(1H)-pyrimidinylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107165-83-3

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107165-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107165-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107165-83:
(8*1)+(7*0)+(6*7)+(5*1)+(4*6)+(3*5)+(2*8)+(1*3)=113
113 % 10 = 3
So 107165-83-3 is a valid CAS Registry Number.

107165-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-2-(1,3-diazinan-2-ylidene)ethanone

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:107165-83-3 SDS

107165-83-3Relevant academic research and scientific papers

Multicomponent Cascade Reaction by Metal-Free Aerobic Oxidation for Synthesis of Highly Functionalized 2-Amino-4-coumarinyl-5-arylpyrroles

Zi, Quan-Xing,Yang, Chang-Long,Li, Kun,Luo, Qin,Lin, Jun,Yan, Sheng-Jiao

supporting information, p. 327 - 338 (2020/01/02)

A novel approach has been constructed for the synthesis of two types of 2-amino-4-coumarinyl-5-arylpyrroles (ACAPs, 5 and 6) through a cascade reaction and a metal-free catalyzed aerobic oxidation reaction of arylglyoxal monohydrates 1, 1,1-enediamines (E

Synthesis of imidazo[1,2-a]pyridines and pyrido[1,2-a]pyrimidines in water and their snar cyclizations

Chanu, Langpoklakpam Gellina,Singh, Thokchom Prasanta,Jang, Yong Ju,Yoon, Yong-Jin,Singh, Okram Mukherjee,Lee, Sang-Gyeong

, p. 994 - 1000 (2014/05/06)

Synthesis of tetrahydroimidazo[1,2-a]pyridines and tetrahydropyrido[1,2-a] pyrimidines by a one-pot and three component reaction of α-oxoketenedithioacetals, diamines and DMAD in water has been described. Different routes for accessing the desired compoun

The synthesis of fluoroheterocyclic ketene aminals

Li,Smith

, p. 527 - 533 (2007/10/03)

The synthesis of fluoroheterocyclic ketene aminals was investigated. Fluorobenzyl ketene dithioacetals 1c reacted with nitric acid in the presence of concentrated sulfuric acid to give compound 2c. 1 reacted with diamines to afford 3-4. C-fluorobenzylatio

SYNTHESIS OF BENZOYL SUBSTITUTED HETEROCYCLIC KETENE AMINALS BY CONDENSATION OF BENZOYL KETENE MERCAPTALS WITH DIAMINES

Huang, Zhi-tang,Liu, Zhi-rong

, p. 943 - 958 (2007/10/02)

2-(Benzoylmethylene)imidazolidines 2 and 5, -hexahydropyrimidines 3 and 6, or -hexahydro-1H-1,3-diazepines 4 were synthesized by the reaction of benzoyl substituted ketene mercaptals 1 with diamines.

Synthesis of 2-(Benzoylmethylene)imidazolidines and -hexahydropyrimidines by Condensation of Ethyl Benzoylacetimidates With 1,2-Ethanediamine or 1,3-Propanediamine, and Some Addition Reactions

Huang, Zhi-tang,Liu, Zhi-rong

, p. 357 - 362 (2007/10/02)

Ethyl benzoylacetimidates react with 1,2-ethanediamine or 1,3-propanediamine in absolute ethanol to afford the 2-(benzoylmethylene)imidazolidines or -hexahydropyrimidines, respectively.The structure of these products as ketene aminals is confirmed by spec

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