15163-60-7

Basic information

• Product Name: Benzoic acid, 4-chloro-, potassium salt
• CAS NO: 15163-60-7
• Molecular Formula: C7H5ClO2.K
• Molecular Weight: 194.659
• Mol File: 15163-60-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-chloro-, potassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-chloro-, potassium salt(15163-60-7)
• EPA Substance Registry System: Benzoic acid, 4-chloro-, potassium salt(15163-60-7)

Safety Data

• Hazardous Substances Data: 15163-60-7(Hazardous Substances Data)

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 
• 201230-82-2 carbon monoxide 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 10519-96-7 potassium trimethylsilonate 
• 74-11-3 para-chlorobenzoic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 2829-26-7 N-(4-chlorobenzylidene)-N'-phenylhydrazine 

Downstream Products

• 790-41-0 4-chlorobenzoic anhydride 
• 15784-28-8 allyl 4-chlorobenzoate 
• 76240-92-1 (4-chlorobenzoyloxymethyl)trifluorosilane 
• 141356-77-6 (S)-2-hydroxyheptyl 4-chlorobenzoate 
• 2655-83-6 1-chloro-3-ethoxybenzene 
• 109842-38-8 dimethyl 2-(4-chlorophenyl)maleate 
• 100446-64-8 1-(4-chlorobenzoyloxymethyl)silatrane 
• 67483-73-2 benzyl p-chlorobenzoate 
• 100-21-0 terephthalic acid 
• 226987-14-0 benzenesulfonic-p-chlorobenzoic anhydride 
• 21961-55-7 benzoic-p-chlorobenzoic anhydride 
• 56741-11-8 methylidene di(4-chlorobenzoate) 
• 6833-15-4 4-chlorobenzanilide 
• 80825-01-0 N-(p-chlorobenzoyl)phthalimide 

Relevant articles and documents

METAL SILANOLATES: ORGANIC SOLUBLE EQUIVALENTS FOR O-2

Alkali metal trimethylsilanolates, M+ -OSiMe3, convert carboxylic acid derivatives into their corresponding anhydrous acid salts under mild non-aqueous conditions.

Facile and direct synthesis of symmetrical acid anhydrides using a newly prepared powerful and efficient mixed reagent

An efficient mixed reagent for direct synthesis of symmetrical carboxylic anhydrides from carboxylic acids has been prepared. Carboxylic acids are converted to anhydrides using triphenylphosphine/ trichloroisocyanuric acid under mild reaction conditions at room temperature. Short reaction time, excellent yields of products, low cost, availability of reagents, simple experimental procedure, and easy work-up of the products are the main advantages of the presented method.

Surfactant-mediated solvent-free dealkylative cleavage of ethers and esters and trans-alkylation under neutral conditions

A simple, surfactant-mediated, one-pot, solvent-free dealkylative cleavage of aryl ethers and esters followed by subsequent optional trans-alkylation under essentially neutral conditions has been developed.