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diethyl (diethylamino)propanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37706-08-4

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37706-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37706-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37706-08:
(7*3)+(6*7)+(5*7)+(4*0)+(3*6)+(2*0)+(1*8)=124
124 % 10 = 4
So 37706-08-4 is a valid CAS Registry Number.

37706-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-(diethylamino)propanedioate

1.2 Other means of identification

Product number -
Other names diethylamino-malonic acid diethyl 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:37706-08-4 SDS

37706-08-4Relevant academic research and scientific papers

Highly efficient sequential N,N,C-trialkylation of α-N-acyloxyimino esters

Mizota, Isao,Maeda, Tatsuya,Shimizu, Makoto

, p. 5793 - 5799 (2015/08/03)

α-N-Acyloxyimino esters serve as highly efficient substrates for the N,N,C-trialkylation reaction that can introduce various patterns of nucleophiles at the imino nitrogen and carbon atoms to synthesize N,N-dialkylated and N,N,C-trialkylated α-amino esters in moderate to high yields.

ORGANIC PHOSPHORUS COMPOUNDS 76 SYNTHESIS AND PROPERTIES OF PHOSPHINOTHRICIN DERIVATIVES

Maier, Ludwig,Lea, Peter J.

, p. 1 - 20 (2007/10/02)

The synthesis, chemical and spectral properties of phosphinothricin analogues which either have other groups than methyl attached to phosphorus (30 to 40) or bear substituents on nitrogen (43 to 50) are described and the activity of some of these derivatives as glutamine synthetase inhibitors and contact herbicides is reported.

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