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2-Propynoic acid, 3-(diethylamino)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17691-75-7

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17691-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17691-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17691-75:
(7*1)+(6*7)+(5*6)+(4*9)+(3*1)+(2*7)+(1*5)=137
137 % 10 = 7
So 17691-75-7 is a valid CAS Registry Number.

17691-75-7SDS

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 3-(diethylamino)propynoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl diethylaminopropiolate

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:17691-75-7 SDS

17691-75-7Relevant 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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