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4H-Pyrido[1,2-a]pyrimidin-4-one, 6,7,8,9-tetrahydro-2-methyl-6-methylene-3-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88499-87-0

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88499-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88499-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88499-87:
(7*8)+(6*8)+(5*4)+(4*9)+(3*9)+(2*8)+(1*7)=210
210 % 10 = 0
So 88499-87-0 is a valid CAS Registry Number.

88499-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl-3 methyl-2 methylene-6 oxo-4 piperidino<1,2-a>pyrimidine

1.2 Other means of identification

Product number -
Other names 3-Benzyl-2-methyl-6-methylene-6,7,8,9-tetrahydro-pyrido[1,2-a]pyrimidin-4-one

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:88499-87-0 SDS

88499-87-0Downstream Products

88499-87-0Relevant academic research and scientific papers

Reactions de cyclisation de pentynyl-2 pyrimidones-4

Rougeot, Etienne,Moskowitz, Henri,Miocque, Marcel

, p. 1407 - 1409 (2007/10/02)

Acetylenic amidines HCC-(CH2)n-C(=NH)NH2 give, by condensation with β-ketoesters, pyrimidones substituted on carbon 2 by an acetylenic chain.Two types of evolution are observed when compounds are heated without any catalyst.The minor route is a cyclization by attack on a triple bond by the amidic nitrogen atom.The main reaction is a cycloaddition involving the non activated triple bond and an azadienic system, leading to non isolated tricyclic intermediates which retrocyclize to stable bicyclic compounds.

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