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359803-53-5

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359803-53-5 Usage

Reactions

A new, air and moisture-stable, palladium catalyst useful in a broad scope of C-C and C-N coupling reactions. The highlyactive catalyst can tolerate substrates containing a wide variety of functional groups such as alkyls, alkoxides, ketones, aldehydes, esters, amines, trifluoromethyl and nitro groups.

Chemical Properties

Light grey powder

Check Digit Verification of cas no

The CAS Registry Mumber 359803-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,8,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 359803-53:
(8*3)+(7*5)+(6*9)+(5*8)+(4*0)+(3*3)+(2*5)+(1*3)=175
175 % 10 = 5
So 359803-53-5 is a valid CAS Registry Number.

359803-53-5SDS

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 [(1R,4S)-3-bicyclo[2.2.1]heptanyl]-[(1S,4R)-3-bicyclo[2.2.1]heptanyl]phosphane,chloropalladium(1+),N,N-dimethyl-2-phenylaniline

1.2 Other means of identification

Product number -
Other names 2'-(dimethylamino)-2-biphenylpalladium(II) chloride dinorbornylphosphine

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:359803-53-5 SDS

359803-53-5Downstream Products

359803-53-5Relevant articles and documents

A new generation of air stable, highly active Pd complexes for C-C and C-N coupling reactions with aryl chlorides

Schnyder, Anita,Indolese, Adriano F.,Studer, Martin,Blaser, Hans-Ulrich

, p. 3668 - 3671 (2007/10/03)

High yields in important Pd-catalyzed reactions of aryl chlorides (see scheme) are obtained with complexes consisting of a palladacycle and a secondary phosphane which could be prepared in situ or isolated. The latter were shown to be stable, and easy to handle in air, and the in situ catalysts allow optimization of the catalyst by variation of the two components.

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