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73283-20-2

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73283-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73283-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73283-20:
(7*7)+(6*3)+(5*2)+(4*8)+(3*3)+(2*2)+(1*0)=122
122 % 10 = 2
So 73283-20-2 is a valid CAS Registry Number.

73283-20-2SDS

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 3-(2-chlorophenyl)-2-(3,3,3-trifluoro-2-oxopropyl)quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 3-(2-Chlorophenyl)-2-(3,3,3-trifluoro-2-oxopropyl)-4(3H)-quinazolinone

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:73283-20-2 SDS

73283-20-2Downstream Products

73283-20-2Relevant articles and documents

2-Ketoalkyl-4(3H)-quinazolinones

-

, (2008/06/13)

2-Ketoalkyl-4(3H)-quinazolinones of the formula STR1 wherein R1 is an aliphatic, cycloaliphatic or hydrocarbon aromatic group of 1-10 carbon atoms; A is divalent alkylene of 1 to 10 carbon atoms; R2 is an aliphatic, cycloaliphatic, hydrocarbon aromatic or heterocyclic group of 1-10 carbon atoms formed by condensing an acyl ester of the formula R2 COOR' which can be dissociated to form --COR2 and R'OH in which R' is the alcoholic portion of said ester; and R3 and R4 are each hydrogen, hydroxy, amino, halogen, trifluoromethyl, alkyl, alkoxy, alkylthio or alkylsulfonyl each of 1-4 carbon atoms, the substituents other than hydrogen when present being preferably in the 6- and/or 7-position of the quinazolinone nucleus provide compounds having useful activity as CNS depressants and anticonvulsants. A process is provided for preparing such compounds by ester condensation of a corresponding 2-alkyl-3-substituted-4(3H) quinazolinone with a condensable ester and excess sodium hydride in the presence of a strong ionization solvent such as refluxing 1,2-dimethoxyethane.

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