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2,3,6,7-tetrahydroimidazo[1,2-a]pyrimidin-5(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15231-34-2

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15231-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15231-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15231-34:
(7*1)+(6*5)+(5*2)+(4*3)+(3*1)+(2*3)+(1*4)=72
72 % 10 = 2
So 15231-34-2 is a valid CAS Registry Number.

15231-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6,7-tetrahydro-1H-imidazo[1,2-a]pyrimidin-5-one

1.2 Other means of identification

Product number -
Other names 5-Keto-2,3,6,7-terahydro-1(H),5(H)-imidazo-(1,2-a)pyrimidin

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:15231-34-2 SDS

15231-34-2Downstream Products

15231-34-2Relevant academic research and scientific papers

The cyclization of 2-substituted imidazolines in sulfuric acid

Cox, Robin A.,Moore, David B.,McDonald, Robert S.

, p. 1910 - 1914 (2007/10/02)

A study of the rates of the cyclizations 1 -> 3 and 2 -> 4 as a function of medium acidity and temperature in aqueous sulfuric acid has been performed.The latter reaction is five times faster at all acidities.An excess acidity kinetic analysis reveals the probable involvement of a water molecule in the reaction in both cases.Mechanistic possibilities suggested by the observations are discussed; it is proposed that the water molecule acts as a base catalyst during the rate-determining ring closure.

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