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4945-42-0

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4945-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4945-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4945-42:
(6*4)+(5*9)+(4*4)+(3*5)+(2*4)+(1*2)=110
110 % 10 = 0
So 4945-42-0 is a valid CAS Registry Number.

4945-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name furo[3,4-b]quinoline-1,3-dione

1.2 Other means of identification

Product number -
Other names quinoline-2,3-dicarboxylic anhydride

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:4945-42-0 SDS

4945-42-0Relevant articles and documents

New efficient access to fused (Het)Aryltetrahydroindolizinones via N-acyl iminium intermediates

Chiurato, Matteo,Boulahjar, Rajaa,Routier, Sylvain,Troin, Yves,Guillaumet, Gérald

scheme or table, p. 4647 - 4653 (2010/07/05)

In this paper, we described the preparation of fused (Het)Aryltetrahydroindolizinones via N-acyl iminium intermediates. Two different routes were also explored to achieve the synthesis. The first one consists in the intramolecular reaction of β-hydroxylactams whereas the second route one is an intermolecular condensation between a 2-formylester or a β-alkoxylactone and an appropriate primary amine. We also developed two heterocyclic strategies to obtain the adequate unavailable starting materials in pyridine, pyrazine, quinoline, and quinaxoline series and then perform all inter or intramolecular reactions. Scope and limitations are given.

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