637353-09-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Chloro-6-(4-chlorophenyl)pyrazine is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique structural features and reactivity.
Used in Agrochemical Development:
2-chloro-6-(4-chlorophenyl)pyrazine is also employed in the creation of agrochemicals, specifically for the development of new insecticides and herbicides, capitalizing on its pesticidal properties to enhance crop protection.
Used in Organic Reactions as a Catalyst:
2-Chloro-6-(4-chlorophenyl)pyrazine has been studied for its potential as a catalyst in organic reactions, leveraging its ability to form coordination complexes with transition metal ions to facilitate and improve the efficiency of certain chemical processes.
Used in Anti-Tumor Research:
Furthermore, 2-chloro-6-(4-chlorophenyl)pyrazine has been investigated for its potential as an anti-tumor agent, indicating its possible use in oncology for the treatment of various cancers, pending further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 637353-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,3,5 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 637353-09:
(8*6)+(7*3)+(6*7)+(5*3)+(4*5)+(3*3)+(2*0)+(1*9)=164
164 % 10 = 4
So 637353-09-4 is a valid CAS Registry Number.
637353-09-4Relevant articles and documents
7-PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES
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Page/Page column 109-110, (2010/07/09)
Compounds of Formula I: (I) in which A, A1, R1, R7a, R7b, R8 and R10 have the meanings given in the specification, are DP2 receptor inhibitors useful in the treatment of useful in the treat
CHEMICAL COMPOUNDS
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Page 52, (2010/02/05)
A compound of formula (I) or a pharmaceutically acceptable salt, solvate, or hydrolysable ester thereof, .Wherein:R1 and R2 are independently hydrogen or C1-3 alkyl;X represents a bond, CH2 or O;R3 and R4 are independently hydrogen, C1-6 alkyl, OCH3, CF3, allyl or halogen;X1 is CH2, SO2, or CO;R5 is -C1-6 alkyl (optionally substituted by C1-6alkoxy or C1-6alkylthio), -C2-6 alkenyl, -C0-6 alkyl phenyl (wherein the phenyl is optionally substituted by one or more CF3, halogen, C1-3 alkyl, C1-3 alkoxy), -COC1-6 alkyl, SO2C1-6 alkyl ;R6 is phenyl or a 6 membered heteroaryl group containing 1,2 or 3 N atoms wherein the phenyl or heteroaryl group is optionally substituted with 1, 2 or 3 moieties selected from the group consisting of C1-6 alkyl, halogen, -OC1-6 alkyl, -SO2C1-3 alkyl, phenyl (optionally substituted by one or more groups selected from halogen, CF3, C1-3 alkyl, OC1-3 alkyl, acetyl, CN).
