37960-65-9

Basic information

• Product Name: Benzoic acid, 2-amino-, monopotassium salt
• CAS NO: 37960-65-9
• Molecular Formula: C7H7NO2.K
• Molecular Weight: 175.228
• Mol File: 37960-65-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-amino-, monopotassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-amino-, monopotassium salt(37960-65-9)
• EPA Substance Registry System: Benzoic acid, 2-amino-, monopotassium salt(37960-65-9)

Safety Data

• Hazardous Substances Data: 37960-65-9(Hazardous Substances Data)

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 118-92-3 anthranilic acid 

Downstream Products

• 89-50-9 2-(ethylamino)benzoic acid 
• 81-78-7 1,5-Bis(2-carboxyanilino)-9,10-anthracenedione 
• 5326-47-6 2-amino-5-iodobenzoic acid 
• 114514-94-2 N-Methoxycarbonylmethylanthranilsaure 
• 19689-08-8 2({4-[(2-carboxyphenyl)amino]-4-oxobutanoyl}amino)benzoicacid 
• 38446-21-8 ethyl 2-(ethylamino)benzoate 
• 87-25-2 2-ethoxycarbonylaniline 
• 86672-47-1 3-(3-Chloro-2-methyl-phenyl)-1H-quinazoline-2,4-dione 
• 101646-18-8 2-carboxymalonanilic acid ethyl ester 
• 579-92-0 Vanadox 
• 6053-45-8 2,2-dimethyl-cyclopentane-1,1,3-tricarboxylic acid 
• 118-92-3 anthranilic acid 
• 2164-95-6 N-phenyl-N'-(2-carboxyphenyl)-urea 
• 603-23-6 3-phenyl-2,4-(1H,3H)-quinazolinedione 

Relevant articles and documents

General Synthesis of Amino Acid Salts from Amino Alcohols and Basic Water Liberating H2

An atom-economical and environmentally friendly method to transform amino alcohols to amino acid salts using just basic water, without the need of pre-protection or added oxidant, catalyzed by a ruthenium pincer complex, is developed. Water is the solvent, the source of the oxygen atom of the carboxylic acid group, and the actual oxidant, with liberation of dihydrogen. Many important and useful natural and unnatural amino acid salts can be produced in excellent yields by applying this new method.

Sulfonium salts and use and preparation thereof

Sulfonium salts of the formula: STR1 wherein Ar is a fused aromatic radical; R1 is a divalent organic bridge; each R2 and R3 individually is an alkyl, aryl, alkaryl, aralkyl or substituted aryl, provided thatn not more than one of R2 and R3 is alkyl; and A is a non-nucleophilic anion; use thereof and preparation thereof.