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4-CHLORO-2-CHLOROMETHYL-5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDINE is a thieno[2,3-d]pyrimidine derivative with a molecular formula C9H9Cl2N3S. It features a heterocyclic ring with two chlorine atoms and two methyl groups attached, exhibiting notable biological activity. This chemical compound is recognized for its potential applications across various industries, particularly in pharmaceuticals and agriculture, due to its antifungal, antimicrobial, antiviral, and anticancer properties.

88203-19-4

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88203-19-4 Usage

Uses

Used in Pharmaceutical Industry:
4-CHLORO-2-CHLOROMETHYL-5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDINE is used as a key intermediate in the synthesis of potential drug candidates for its demonstrated biological activity. It is particularly valued for its potential antifungal and antimicrobial properties, making it a candidate for developing new treatments against various infections.
Used in Antiviral Applications:
In the field of virology, 4-CHLORO-2-CHLOROMETHYL-5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDINE is explored as an antiviral agent, leveraging its ability to combat viral infections and contributing to the development of novel antiviral medications.
Used in Anticancer Applications:
4-CHLORO-2-CHLOROMETHYL-5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDINE is also being studied for its potential as an anticancer agent, with research focusing on its capacity to target and inhibit the growth of cancer cells, offering a new avenue for cancer treatment.
Used in Agricultural Industry:
4-CHLORO-2-CHLOROMETHYL-5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDINE has been investigated for its potential as a herbicide, suggesting that it could be utilized in the agricultural sector to control weed growth, thereby increasing crop yields and protecting agricultural land.

Check Digit Verification of cas no

The CAS Registry Mumber 88203-19-4 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 88203-19:
(7*8)+(6*8)+(5*2)+(4*0)+(3*3)+(2*1)+(1*9)=134
134 % 10 = 4
So 88203-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2N2S/c1-4-5(2)14-9-7(4)8(11)12-6(3-10)13-9/h3H2,1-2H3

88203-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2-(chloromethyl)-5,6-dimethylthieno[2,3-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 4-Chloro-2-chloromethyl-5,6-dimethyl-thieno[2,3-d]pyrimidine

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:88203-19-4 SDS

88203-19-4Downstream Products

88203-19-4Relevant academic research and scientific papers

Synthesis and antihyperlipidemic activity of some novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-disubstituted pyrimidines

Kathiravan, Matthu K.,Shishoo, Chamanlal J.,Kumar, Krishnan Girish,Roy, Saroj Kumar,Mahadik, Kakasheb R.,Kadam, Shivajirao S.,Jain, Kishor S.

, p. 599 - 606 (2008/03/13)

Synthesis and antihyperlipidemic activity of a series of novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-di-substituted pyrimidines are described. The design of these compounds is based on the earlier QSAR study on the antihyperlipidemic 2-substituted

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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