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1789-01-1

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1789-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1789-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1789-01:
(6*1)+(5*7)+(4*8)+(3*9)+(2*0)+(1*1)=101
101 % 10 = 1
So 1789-01-1 is a valid CAS Registry Number.

1789-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-aminophenyl)-2-methylquinazolin-4-one

1.2 Other means of identification

Product number -
Other names B 226

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:1789-01-1 SDS

1789-01-1Downstream Products

1789-01-1Relevant articles and documents

Expeditious synthesis and spectroscopic characterization of 2-methyl-3-substituted-quinazolin-4(3H)-one derivatives

Ajani, Olayinka O.,Audu, Oluwatosin Y.,Germann, Markus W.,Bello, Babatunde L.

, p. 562 - 574 (2017/05/26)

Quinazoline and quinazolinone derivatives are well-known bioactive heterocycles owing to their therapeutic diversity and extensive medicinal application in drug design and pharmaceutics. A series of 2-methyl-3-substituted quinazolin-4(3H)-one derivatives 8a-q was herein synthesized from synthetic conversion of anthranilic acid to 2-methyl-4H-3,1-benzoxazi-4-one, 7 which was subsequently transformed to the targeted 2,3-disubstituted quinazolin-4(3H)-one derivatives 8a-q by reacting with some notable amino-containing moieties via an ameliorable pathway. The catalyst-free synthesis was successful achieved by careful reaction optimization study using solvent choice and reaction temperature variability as key parameters. The chemical structures of the synthesized compounds were confirmed by IR, UV, 1H-NMR, 13C-NMR and DEPT-135 as well as analytical data.

SUBSTITUTED 4-QUINAZOLINONE DERIVATIVES AS HYPNOTICS AND

BOLTZE,DELL,LEHWALD,LORENZ,RUEBERG-SCHWEER

, p. 688 - 701 (2007/10/04)

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