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144463-84-3

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144463-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144463-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144463-84:
(8*1)+(7*4)+(6*4)+(5*4)+(4*6)+(3*3)+(2*8)+(1*4)=133
133 % 10 = 3
So 144463-84-3 is a valid CAS Registry Number.

144463-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2'methylphenyl)-quinoline-3,4-dicarboxylic anhydride

1.2 Other means of identification

Product number -
Other names -

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:144463-84-3 SDS

144463-84-3Relevant articles and documents

Pyrolysis of quinoline-3,4-dicarboxylic anhydrides bearing 2-phenyl, 2-benzyl and 2-o-tolyl substituents: Formation of products of carbene insertion and addition

Brown,Coulston,Eastwood,Moffat

, p. 7763 - 7774 (2007/10/02)

Flash vacuum pyrolysis of 2-phenylquinoline-3,4-dicarboxylic anhydride at 800°/0.06 mm gave indeno[1,2-b]indole (30-40%), which readily added nucleophiles Y- at C-10 to give 5,10-dihydro derivatives (Y=H, Me, Ph, NEt2, OMe, CH(COOMe)2 and CMe2NO2). Similar pyrolysis of the 2-benzylquinoline anhydride gave a 1:2 mixture of the (expected) linear 5H-benzo[b]carbazole and the (unexpected) angular 7H-benzo[c]carbazole. The isomeric 2-o-tolylquinoline anhydride on similar pyrolysis gave mainly 11H-benzo[a]carbazole (85%), isomeric benzocarbazoles (4%) and 11H-indeno[1,2-b]quinoline (2.6%). Most of these products are probably derived from exocyclic carbenes formed by aryne-carbene equilibration, but the last compound may be formed by direct aryne-methyl interaction.

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