1346435-43-5

Basic information

• Product Name: 1-chloro-3-(3-(oxiran-2-ylmethoxy)phenoxy)propan-2-ol
• Synonyms: 1-chloro-3-(3-(oxiran-2-ylmethoxy)phenoxy)propan-2-ol
• CAS NO: 1346435-43-5
• Molecular Weight: 258.702
• Mol File: 1346435-43-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-chloro-3-(3-(oxiran-2-ylmethoxy)phenoxy)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-chloro-3-(3-(oxiran-2-ylmethoxy)phenoxy)propan-2-ol(1346435-43-5)
• EPA Substance Registry System: 1-chloro-3-(3-(oxiran-2-ylmethoxy)phenoxy)propan-2-ol(1346435-43-5)

Safety Data

• Hazardous Substances Data: 1346435-43-5(Hazardous Substances Data)

Upstream product

• 106-89-8 epichlorohydrin 
• 108-46-3 recorcinol 
• 101-90-6 resorcinol diglycidyl ether 

Downstream Products

• 1346435-42-4 2,2-dimethyl-propionic acid 2-{3-[3-chloro-2-(2,2-dimethyl-propionyloxy)-propoxy]-phenoxy}-1-chloromethyl-ethyl ester 
• 1346435-44-6 2,2-dimethyl-propionic acid 2-[3-(3-chloro-2-hydroxy-propoxy)-phenoxy]-1-chloromethyl-ethyl ester 
• 1346435-41-3 2,2-dimethyl-propionic acid 1-chloromethyl-2-(3-oxiranylmethoxy-phenoxy)-ethyl ester 

Relevant articles and documents

Study of the O-glycidylation of natural phenolic compounds. the relationship between the phenolic structure and the reaction mechanism

The O-alkylation reaction by epichlorohydrin of some natural phenolic compounds such as 4-methylcatechol, gallic acid, protocatechuic acid, pyrogallol and resorcinol was investigated. Phenolic compounds reacted first with epichlorohydrin in the presence of benzyltriethylammonium chloride as phase transfer catalyst. Then, an aqueous solution of sodium hydroxide was added. It was demonstrated that the two competitive mechanisms involved in the O-alkylation reaction were highly dependent of the starting material. The O-alkylated products obtained in this reaction could be further used as bisphenol A substitutes in the synthesis of epoxy resins pre-polymers.