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20802-02-2

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20802-02-2 Usage

Physical State

Colorless liquid

Uses

+ Intermediate in the production of various organic compounds
+ Ingredient in fragrances and flavorings
+ Solvent in industrial processes

Safety Precautions

Skin and eye irritant; should be handled in a controlled environment.

Check Digit Verification of cas no

The CAS Registry Mumber 20802-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20802-02:
(7*2)+(6*0)+(5*8)+(4*0)+(3*2)+(2*0)+(1*2)=62
62 % 10 = 2
So 20802-02-2 is a valid CAS Registry Number.

20802-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-[1-(4-methoxyphenyl)prop-1-en-2-yl]benzene

1.2 Other means of identification

Product number -
Other names 1,2-Di-(p-anisyl)-propen-(1)

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:20802-02-2 SDS

20802-02-2Relevant articles and documents

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

Kondolff, Isabelle,Doucet, Henri,Santelli, Maurice

, p. 8487 - 8491 (2007/10/03)

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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