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33149-48-3

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33149-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33149-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33149-48:
(7*3)+(6*3)+(5*1)+(4*4)+(3*9)+(2*4)+(1*8)=103
103 % 10 = 3
So 33149-48-3 is a valid CAS Registry Number.

33149-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl[1]benzofuro[3,2-d]pyrimidin-4(1H)-one

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-2-methyl-4-oxobenzofuro<3,2-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:33149-48-3 SDS

33149-48-3Relevant articles and documents

THIENO[2,3-D)PYRIMIDINES AND BENZOFURO(3,2-D)PYRIMIDINES AS ANTIMICROBIAL AGENTS

-

, (2019/02/06)

The present disclosure provides compounds, methods, and compositions which may be used to treat tuberculosis. In some embodiments, these compounds and compositions have a bactericidal property against Mycobacterium tuberculosis (Mtb). Methods of employing such agents are also provided.

Studies in Benzofurans : Part VIII-Synthesis of Some 3-N-aryl-, 3-N-Alkyl- and 3-Amino-3,4-dihydro-4-oxobenzofuropyrimidines

Mahajan, S. B.,Agasimundin, Y. S.

, p. 402 - 404 (2007/10/02)

Ethyl 3-amino-2-benzofuran-carboxylate (I) on condensation with ethyl orthoformate and various aromatic amines affords 3-N-aryl-3,4-dihydro-4-oxobenzofuropyrimidines (II).Analogous 3-alkyl and 3-amino compounds have been prepared by the reaction of ethyl 3-(ethoxymethylene)amino-2-benzofurancarboxylate (III) with aliphatic amines and hydrazine hydrate respectively.

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