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4-chloro-2-(dichloromethyl)quinazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88203-16-1

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88203-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88203-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88203-16:
(7*8)+(6*8)+(5*2)+(4*0)+(3*3)+(2*1)+(1*6)=131
131 % 10 = 1
So 88203-16-1 is a valid CAS Registry Number.

88203-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2-(dichloromethyl)quinazoline

1.2 Other means of identification

Product number -
Other names 4-chloro-2-(dichloro-methyl)-quinazoline

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:88203-16-1 SDS

88203-16-1Downstream Products

88203-16-1Relevant academic research and scientific papers

Sonogashira cross-coupling reaction in 4-chloro-2- trichloromethylquinazoline series is possible despite a side dimerization reaction

Kieffer, Charline,Verhaeghe, Pierre,Primas, Nicolas,Castera-Ducros, Caroline,Gellis, Armand,Rosas, Roselyne,Rault, Sylvain,Rathelot, Pascal,Vanelle, Patrice

, p. 2987 - 2995 (2013/03/29)

We studied the Sonogashira coupling reaction between 4-chloro-2- trichloromethylquinazoline and various terminal alkynes, mainly in phenylacetylene series. A brief review of the literature shows that mono- or polybromo/chloromethylated substrates, especia

Reaction of Nitriles under Acidic Conditions. Part VI. Synthesis of Condensed 4-Chloro- and 4-Aminopyrimidines from ortho-Aminonitriles

Shishoo, C. J.,Devani, M. B.,Bhadti, V. S,Jain, K. S.,Ananthan, S.

, p. 119 - 126 (2007/10/02)

Condensation of a nitrile with benzene, furan and thiophene ortho-aminonitriles in the presence of dry hydrogen chloride yields condensed 4-chloropyrimidines, condensed 4-aminopyrimidines or a mixture of the two condensed pyrimidines in varying proportions depending upon the nature of the nitrile and the substrate, ortho-aminonitrile.

REACTION OF NITRILES UNDER ACIDIC CONDITIONS: A NOVEL, DIRECT FORMATION OF CONDENSED 4-CHLOROPYRIMIDINES

Shishoo, C. J.,Devani, M. B.,Bhadti, V. S.,Anathan, S.,Ullas, G. V.

, p. 4611 - 4612 (2007/10/02)

An unusual formation of condensed 4-chloropyrimidines in the reaction of o-aminonitriles with halogenoacetonitriles in the presence of dry hydrogen chloride gas is described.

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