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120543-33-1

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120543-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120543-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,4 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120543-33:
(8*1)+(7*2)+(6*0)+(5*5)+(4*4)+(3*3)+(2*3)+(1*3)=81
81 % 10 = 1
So 120543-33-1 is a valid CAS Registry Number.

120543-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium 4-cyanobenzoate

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:120543-33-1 SDS

120543-33-1Relevant articles and documents

SYNTHESIS OF ARENECARBOXYLIC ACIDS FROM ARYL IODIDES

Bumagin, N. A.,Nikitin, K. V.,Beletskaya, I. P.

, p. 1286 (1988)

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Decarboxylative cross-coupling of aryl tosylates with aromatic carboxylate salts

Goossen, Luksa J.,Rodriguez, Nuria,Lange, Paul P.,Linder, Christophe

supporting information; experimental part, p. 1111 - 1114 (2010/04/29)

(Figure Presented) A bimetallic copper/palladium catalyst system is disclosed that enables the use of tosylates as carbon electrophiles in decarboxylative coupling reactions. A variety of aromatic carboxylate salts, regardless of their substitution pattern, have been coupled with these inexpensive and readily available electrophiles to give the corresponding biaryl compounds in good yields (see scheme).

Decarboxylative biaryl synthesis from aromatic carboxylates and aryl triflates

Goossen, Lukas J.,Rodriguez, Nuria,Linder, Christophe

supporting information; experimental part, p. 15248 - 15249 (2009/03/11)

A new catalyst system, generated in situ from Cu2O, 1,10-phenanthroline, PdI2, and Tol-BINAP, for the first time allows the decarboxylative coupling of carboxylic acids with aryl triflates. In contrast to previous decarboxylative couplings that remained limited to certain activated carboxylates, e.g., ortho-substituted benzoates, this halide-free protocol is generally applicable to aromatic carboxylic acid salts regardless of their substitution pattern. Copyright

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