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15922-01-7

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15922-01-7 Usage

General Description

4-Nitrobenzoic acid potassium salt is a chemical compound with the formula C7H4NO4K. It is a potassium salt of 4-nitrobenzoic acid, which is commonly used as a precursor for the synthesis of various pharmaceuticals, dyes, and pesticides. It is a yellow crystalline solid that is slightly soluble in water and has a melting point of 340°C. 4-NITROBENZOIC ACID POTASSIUM SALT is mainly used in organic synthesis and as an intermediate in the production of other chemicals. Additionally, it has potential applications in the field of polymer science and materials chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 15922-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15922-01:
(7*1)+(6*5)+(5*9)+(4*2)+(3*2)+(2*0)+(1*1)=97
97 % 10 = 7
So 15922-01-7 is a valid CAS Registry Number.

15922-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Potassium 4-Nitrobenzoate

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:15922-01-7 SDS

15922-01-7Relevant articles and documents

Efficient Method for Aromatic-Aldehyde Oxidation by Cleavage of Their Hydrazones Catalysed by Trimethylsilanolate

Burglova, Kristyna,Okorochenkov, Sergei,Budesinsky, Milos,Hlavac, Jan

, p. 389 - 396 (2017/01/24)

The reactions of hydrazones, derived from various aromatic aldehydes bound to Rink resin and hydrazines, with trimethylsilanolate have been studied. In this process, the aldehydes were oxidized to the corresponding carboxylic acids. The reaction was also tested with success in solution, with various aromatic aldehydes easily being oxidized in one pot via hydrazone formation and trimethylsilanolate treatment. A mechanism for the hydrazone cleavage is proposed. The reaction may be used as an alternative method for aldehyde oxidation with the selectivity complementary to that of currently used reactions.

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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