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2-Propynoic acid, 3-(dimethylamino)-, methyl ester is a chemical compound with the molecular formula C7H9NO2. It is an organic ester derived from 2-propynoic acid, featuring a dimethylamino group at the 3-position and a methyl ester group at the 2-position. 2-Propynoic acid, 3-(dimethylamino)-, methyl ester is characterized by its unique structure, which includes a triple bond (acetylene) in the propynoic acid backbone and an amino group that is dimethylated. It is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the development of compounds with biological activity. The compound's properties, such as its reactivity and solubility, make it a valuable building block in organic chemistry.

20570-45-0

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20570-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20570-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,7 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20570-45:
(7*2)+(6*0)+(5*5)+(4*7)+(3*0)+(2*4)+(1*5)=80
80 % 10 = 0
So 20570-45-0 is a valid CAS Registry Number.

20570-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)propynoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl dimethylaminopropiolate

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:20570-45-0 SDS

20570-45-0Relevant academic research and scientific papers

YNAZIRIDINES. METHODS OF SYNTHESIS OF A NEW TYPE OF YNAMINES

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

, p. 1231 - 1235 (2007/10/02)

Ways of synthesizing ynaziridines by succesive halogenation and dehydrohalogenation of enaziridino esters, the reaction of potassium aziridinide with bromophenylacetylene, the reaction of 1H-aziridines with the methyl ester of bromopropionic acid was studied.The different direction of the reaction of aziridines with bromomethylpropiolate as a function of the nature of the solvent was demonstrated.In methanol the addition of aziridine to the triple bond proceeds stereospecifically with the formation of the E-isomer.When this reaction was conducted in ether, ynaziridines were obtained for the first time.An effective method of synthesis of ynaminoesters was developed.

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