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2-Methylpropionimodic acid ethyl ester, also known as ethyl 2-methylpropionimidoate, is an organic compound with the chemical formula C6H11NO2. It is a colorless liquid with a molecular weight of 129.16 g/mol. This ester is derived from 2-methylpropionimidoic acid and is formed by the reaction of the acid with ethanol in the presence of a catalyst. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is characterized by its ester functional group, which contributes to its reactivity and potential applications in chemical transformations.

1069-52-9

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1069-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1069-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1069-52:
(6*1)+(5*0)+(4*6)+(3*9)+(2*5)+(1*2)=69
69 % 10 = 9
So 1069-52-9 is a valid CAS Registry Number.

1069-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-methylpropanimidate

1.2 Other means of identification

Product number -
Other names Isobutyrimidsaeureethylester

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:1069-52-9 SDS

1069-52-9Downstream Products

1069-52-9Relevant academic research and scientific papers

Process for the production of 2-alkyl- or cycloalkyl-4-methyl-6-hydroxypyrimidines

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, (2008/06/13)

Production of 2-alkyl- or cycloalkyl-4-methyl-6-hydroxypyrimidines by first neutralizing an alkyl imidate ester hydrochloride with a base in the presence of a water-immiscible solvent for the alkyl imidate ester to be freed thereby; condensing the alkyl imidate ester with diketene to form an oxazinone intermediate, which is then reacted in organic solution with gaseous ammonia and recovering the desired substituted 6-hydroxypyrimidine.

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