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915302-21-5

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915302-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 915302-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 915302-21:
(8*9)+(7*1)+(6*5)+(5*3)+(4*0)+(3*2)+(2*2)+(1*1)=135
135 % 10 = 5
So 915302-21-5 is a valid CAS Registry Number.

915302-21-5SDS

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 2-chloropyrido[3,2-d]pyrimidine

1.2 Other means of identification

Product number -
Other names Pyrido[3,2-d]pyrimidine,2-chloro

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:915302-21-5 SDS

915302-21-5Relevant articles and documents

INDOLE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS

-

Page/Page column 40; 59, (2022/02/05)

Provided herein are compounds of formula (V) that bind to BF3 of an androgen receptor (AR), which can modulate the AR for the treatment of Kennedy's disease.

Efficient synthesis of 2-substituted pyrido[3,2-d]pyrimidines involving SNAr and palladium-catalyzed cross-coupling reactions

Tikad, Abdellatif,Routier, Sylvain,Akssira, Mohamed,Leger, Jean-Michel,Jarry, Christian,Guillaumet, Gerald

scheme or table, p. 2379 - 2384 (2010/02/27)

The efficient and original synthesis of various 2-substituted pyrido[3,2-d]pyrimidines is reported. Starting from 2,4-dichloropyrido [3,2-d]pyrimidine, a regioselective pallado-dehalogenation led to 2-chloropyrido[3,2-d]pyrimidine, which was used in SNAr and palladium-catalyzed cross-coupling reactions in order to afford highly functionalized products in very good yields. Georg Thieme Verlag Stuttgart.

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