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637352-85-3

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637352-85-3 Usage

General Description

2-CHLORO-6-(4-METHYLPHENYL)PYRAZINE is a chemical compound with the molecular formula C11H9ClN2. It is a heterocyclic organic compound and belongs to the pyrazine class of chemicals. This chemical is a pale yellow to brown liquid with a molecular weight of 208.65 g/mol. It is primarily used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block in organic synthesis and as a reagent in chemical research. 2-CHLORO-6-(4-METHYLPHENYL)PYRAZINE is known for its potential as an anticancer agent and is currently being studied for its pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 637352-85-3 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 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 637352-85:
(8*6)+(7*3)+(6*7)+(5*3)+(4*5)+(3*2)+(2*8)+(1*5)=173
173 % 10 = 3
So 637352-85-3 is a valid CAS Registry Number.

637352-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-6-(4-methylphenyl)pyrazine

1.2 Other means of identification

Product number -
Other names Pyrazine,2-chloro-6-(4-methylphenyl)

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:637352-85-3 SDS

637352-85-3Relevant articles and documents

Use of N-oxide compounds in coupling reactions

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Page/Page column 27-28, (2008/12/05)

Metal-catalyzed coupling process comprising reacting a compound of general formula 1 with a compound A-X, to obtain a compound of general formula 2, which may further be converted to a compound of general formula 3

CHEMICAL COMPOUNDS

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Page 42, (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).

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