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32743-31-0

32743-31-0

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32743-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32743-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,4 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32743-31:
(7*3)+(6*2)+(5*7)+(4*4)+(3*3)+(2*3)+(1*1)=100
100 % 10 = 0
So 32743-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9N3O2/c12-10(15)7-5-9(11(13)16)14-8-4-2-1-3-6(7)8/h1-5H,(H2,12,15)(H2,13,16)

32743-31-0SDS

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 quinoline-2,4-dicarboxamide

1.2 Other means of identification

Product number -
Other names quinoline-2,4-dicarboxylic acid diamide

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:32743-31-0 SDS

32743-31-0Downstream Products

32743-31-0Relevant articles and documents

POLAR EFFECTS IN FREE-RADICAL REACTIONS. NEW SYNTHETIC DEVELOPMENTS IN THE FUNCTIONALIZATION OF HETEROAROMATIC BASES BY NUCLEOPHILIC RADICALS

Minisci, Francesco,Citterio, Attilio,Vismara, Elena,Giordano, Claudio

, p. 4157 - 4170 (2007/10/02)

The synthetic interest of the direct substitution of protonated heteroaromatic bases by nucleophilic carbon-centered radicals is furtheron developed by the following new achievements: i) utilization of the redox system N(+)H3OH/Ti(III) in several solvents; ii) utilization of benzoyl peroxide in alcohols; iii) carbamoylation by HCONH2 and H2O2 in the presence of catalytic amounts of Fe(II).These systems allow to obtain either substitution till now tried without success or reactions of industrial interest.Polar effects play a dominat role in determining reactivity, selectivity and synthetic applications; in particular the role of the strongly nucleophilic intermediate radicals of pyridinyl type in the rearomatization step is emphasized.

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