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2-Propenenitrile, 2-(dimethylamino)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55915-65-6

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55915-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55915-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55915-65:
(7*5)+(6*5)+(5*9)+(4*1)+(3*5)+(2*6)+(1*5)=146
146 % 10 = 6
So 55915-65-6 is a valid CAS Registry Number.

55915-65-6SDS

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 2-(dimethylamino)-3-phenylprop-2-enenitrile

1.2 Other means of identification

Product number -
Other names -

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:55915-65-6 SDS

55915-65-6Downstream Products

55915-65-6Relevant academic research and scientific papers

α-SUBSTITUIERTE PHOSPHONATE 50. Electrochemisch generierte Basen als Reagenz fuer die Horner-Reaktion

Costisella, Burkhard,Gross, Hans,Jeroschewski, Paul,Keitel, Iris,Schwarz, Karl-Heinz

, p. 159 - 164 (2007/10/02)

The radical anion 2 (electrochemically generated base), formed by electrochemical reduction of azobenzene (probase), is suitable for deprotonation of differently substituted phosphonates 4. α-Phosphonyl aniones 5, obtained by such approach, reacted in situ with carbonyl compounds to give α-substituted olefines 6.Similar reaction took place with stilbene as probase.---Side reactions with the solvent were observed with less acidic phosphonates, e.g. 4h.

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