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62732-46-1

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62732-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62732-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,3 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62732-46:
(7*6)+(6*2)+(5*7)+(4*3)+(3*2)+(2*4)+(1*6)=121
121 % 10 = 1
So 62732-46-1 is a valid CAS Registry Number.

62732-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-6,7-dihydro-5H-cyclopenta[b]pyridin-4-amine

1.2 Other means of identification

Product number -
Other names 4-Amin0-2,3-dimethyl-6,7-dihydro-5H-1-pyrindine hydrate

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:62732-46-1 SDS

62732-46-1Downstream Products

62732-46-1Relevant articles and documents

Recyclization of 2,2-Disubstituted 4(3H)-Oxo- and 4-Chloro-1,2-dihydropyrimidines to 4-Aminopyridine Derivatives

Upadysheva, A. V.,Grigor'eva, N. D.,Ryabokobylko, Yu. S.,Znamenskaya, A. P.

, p. 95 - 99 (2007/10/02)

The intramolecular cationotropic rearrangement of salts of two-ring 2,2-disubstituted 4-chloro-1,2-dihydropyrimidines to 4-aminopyrimidine derivatives was observed.Recyclization to 4-aminopyridines can take place in the reaction of two-ring 2,2-disubstituted 4(3H)-oxo-1,2-dihydropyrimidines with phosphorus oxychloride without isolation of the intermediate chloro derivatives.A probable mechanism that makes it possible to assert that the observed recyclization is a variant of the intramolecular cationotropic rearrangement that is characteristic for 2,2-dialkylsubstituted 1,2-dihydropyrimidines with functional substituents (for example, oxo or chloro) in the 4 position of the ring is discussed.

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