35535-81-0

Basic information

• Product Name: sodium 2-chlorophenolate
• Synonyms: sodium 2-chlorophenolate;Sodium 2-chlorobenzene-1-olate;Sodium 2-chlorophenoxide;Caswell no. 203a;Einecs 252-608-2;Epa pesticide chemical code 062205;o-Chlorophenol sodium salt;Phenol, 2-chloro-, sodium salt
• CAS NO: 35535-81-0
• Molecular Formula: C₆H₄ClO*Na
• Molecular Weight: 150.53813
• EINECS: 252-608-2
• Mol File: 35535-81-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 175°Cat760mmHg
• Flash Point: 63.9°C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: sodium 2-chlorophenolate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 2-chlorophenolate(35535-81-0)
• EPA Substance Registry System: sodium 2-chlorophenolate(35535-81-0)

Safety Data

• Hazardous Substances Data: 35535-81-0(Hazardous Substances Data)

Upstream product

• 95-57-8 2-monochlorophenol 

Downstream Products

• 2689-07-8 2-chlorodiphenyl ether 
• 59288-78-7 2-chlorophenyl dimethyl phosphate 
• 32565-14-3 ethyl 2-(2-chlorophenoxy)-3-oxobutanoate 
• 32565-15-4 o-Chlorphenyl-O-acetylessigsaeure 
• 95-57-8 2-monochlorophenol 
• 70771-66-3 sodium 3-chloro-2-hydroxybenzoate 
• 28222-03-9 2-(2-Chlorophenoxy)-5-nitropyridine 
• 91664-74-3 2-(2-chlorophenoxy)thiazoline 
• 13788-46-0 dibutyl 2-chlorophenyl thiophosphate 
• 13677-62-8 Thiophosphorsaeure-di-O-aethylester-O-<2-chlor-phenylester> 
• 1087388-31-5 rac-3-(2-chlorophenoxy)-2-hydroxypropanoic acid 
• 1610620-90-0 S-3-(2-chlorophenoxy)-2-hydroxypropanoic acid 

Relevant articles and documents

Synthesis of enantiomerically pure 3-aryloxy-2-hydroxypropanoic acids, intermediate products in the synthesis of cis-4-Aminochroman-3-ols

Oxidation of accessible (R)-3-chloropropane-1,2-diol to (R)-3-chloro-2-hydroxypropanoic acid and subsequent reaction of the latter with ortho-substituted sodium phenoxide gave a number of enantiomerically pure 3-aryloxy-2-hydroxypropanoic acid which are intermediate products in the synthesis of nonracemic 4-aminochroman-3-ols.

Process for the manufacture of anhydrous alkali metal arylate solutions and separation of the arylates from alkali metal sulfite

Anhydrous organic solutions of alkali metal arylates are prepared by dissolving an alkali metal arylate or reacting an arylhydroxy compound with alkali metal hydroxide in a ketone immiscible or incompletely miscible with water at room temperature and removing the water from the solution, if any, by azeotropic distillation with reflux.