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2-Propen-1-amine, N,N-diethyl-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19737-36-1

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19737-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19737-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19737-36:
(7*1)+(6*9)+(5*7)+(4*3)+(3*7)+(2*3)+(1*6)=141
141 % 10 = 1
So 19737-36-1 is a valid CAS Registry Number.

19737-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-2-methylprop-2-en-1-amine

1.2 Other means of identification

Product number -
Other names Diaethyl-methallyl-amin

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:19737-36-1 SDS

19737-36-1Relevant academic research and scientific papers

Synthetic and kinetic aspects of nickel-catalysed amination of allylic alcohol derivatives

Bricout, Herve,Carpentier, Jean-Francois,Mortreux, Andre

, p. 1073 - 1084 (2007/10/03)

The design of efficient nickel-based catalytic systems for coupling of diethylamine (1) with esters and ether derivatives of allyl alcohol (2a-c) and related allyl-substituted compounds (4a-e) is reported. Special attention is paid to solvent and salt effects on catalytic activities and kinetic profiles for the formation of allyllamines. The results are discussed in terms of the influence of some reaction parameters (polarity, ion exchange processes, substrate) on the rate determining step of the catalytic cycle.

Palladium-Catalyzed Double and Single Carbonylation of Aryl Halides and Allylic Compounds

Yamamoto, Akio

, p. 433 - 446 (2007/10/02)

After a brief introduction summarizing the author's previous work concerning the double carbonylation of aryl halides catalyzed by palladium complexes, newly found catalytic processes (1) for converting allylic formates and chlorides into β,γ-unsaturated acids and (2) the double carbonylation of allylic chlorides to β,γ-unsaturated α-keto amides are described.Mechanisms which reasonably account for the catalytic processes are proposed on the basis of studies concerning the properties of the organopalladium complexes.

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