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Acetic acid, 2-imidazolidinylidene-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98236-82-9

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98236-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98236-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98236-82:
(7*9)+(6*8)+(5*2)+(4*3)+(3*6)+(2*8)+(1*2)=169
169 % 10 = 9
So 98236-82-9 is a valid CAS Registry Number.

98236-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-imidazolidin-2-ylideneacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,2-imidazolidinylidene-,methyl ester

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:98236-82-9 SDS

98236-82-9Downstream Products

98236-82-9Relevant academic research and scientific papers

REACTION OF METHYL BROMOPROPIOLATE WITH DIAMINES AS A METHOD OF SYNTHESIS OF IMIDAZOLIDINE DERIVATIVES

Tikhomirov, D. A.,Slyadevskaya, O. S.,Eremeev, A. V.

, p. 966 - 969 (2007/10/02)

A convenient method of synthesis of 2-(methoxycarbonylmethylene)-substituted imidazolidines and imidazolidinium bromides, and also of bicyclic diazo compounds has been developed starting from methyl bromopropiolate and ethylenediamine and its derivatives.

YNAZIRIDINES AND THEIR REACTIONS WITH AMINES

Shubina, Yu. V.,Tikhomirov, D. A.,Eremeev, A. V.

, p. 516 - 520 (2007/10/02)

On the basis of the results of IR and UV spectroscopy, a considerable decrease in the efficacy of the conjugation of the unshared pair of the nitrogen atom with a carbonyl group in ynaziridines as compared with ynamines has been shown.The difference in the electronic structures of these compounds finds its reflection in their chemical behavior: the electrophilicity of the triple bond in an ynaziridine is higher than that in the analogous ynamine in reaction with amines.

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