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Benzenamine, N,N-dimethyl-4-(2-phenyl-1-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60623-86-1

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60623-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60623-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,2 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60623-86:
(7*6)+(6*0)+(5*6)+(4*2)+(3*3)+(2*8)+(1*6)=111
111 % 10 = 1
So 60623-86-1 is a valid CAS Registry Number.

60623-86-1SDS

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-dimethyl-4-(2-phenylprop-1-enyl)aniline

1.2 Other means of identification

Product number -
Other names 1-(p-Dimethylamino)-2-phenyl-prop-1-en

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:60623-86-1 SDS

60623-86-1Downstream Products

60623-86-1Relevant academic research and scientific papers

Tetraphosphine/palladium-catalyzed Heck reactions of aryl halides with disubstituted alkenes

Kondolff, Isabelle,Doucet, Henri,Santelli, Maurice

, p. 8487 - 8491 (2003)

cis,cis,cis-1,2,3,4-Tetrakis(diphenylphosphinomethyl)cyclopentane/ [PdCl(C3H5)]2 efficiently catalyses the Heck reaction of disubstituted alkenes such as methyl crotonate, ethyl cinnamate, methyl methacrylate or α-methylstyrene with a variety of aryl halides. In the presence of 1,2-disubstituted alkenes the stereoselectivities of the reactions strongly depend on the substituents of the alkenes. Selectivities up to 97% in favor of E-isomers can be obtained for the addition to methyl crotonate. With the 1,1-disubstituted alkenes methyl methacrylate or α-methylstyrene mixtures of products are obtained.

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