67964-17-4

Basic information

• Product Name: (S)_P(-)-O-ethyl phenylphosphonothioic acid
• Synonyms: (S)_P(-)-O-ethyl phenylphosphonothioic acid
• CAS NO: 67964-17-4
• Molecular Weight: 202.214
• Mol File: 67964-17-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)_P(-)-O-ethyl phenylphosphonothioic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)_P(-)-O-ethyl phenylphosphonothioic acid(67964-17-4)
• EPA Substance Registry System: (S)_P(-)-O-ethyl phenylphosphonothioic acid(67964-17-4)

Safety Data

• Hazardous Substances Data: 67964-17-4(Hazardous Substances Data)

Upstream product

• 6231-03-4 diethyl phenylphosphonothioate 
• 6230-93-9 O-ethyl phenylphosphonothioic acid 
• 6230-64-4 O-Ethyl hydrogen phenylphosphonothioate dicyclohexylammonium salt 
• 172487-18-2 ethyl Phenylphosphinate 

Downstream Products

• 1351790-99-2 C₁₀H₁₅O₂PS 
• 1351791-00-8 C₁₀H₁₅O₂PS 
• 123278-21-7 S-methyl O-ethyl ohenylphosphonothioate 
• 61733-60-6 (S)-O-ethyl O-methyl phenylphosphonothioate 
• 61733-60-6 (R)-O-ethyl O-methyl phenylphosphonothioate 
• 6230-64-4 (S)-(-)-O-Ethyl hydrogen phenylphosphonothioate dicyclohexylammonium salt 
• 6230-64-4 (R)-(+)-O-Ethyl hydrogen phenylphosphonothioate dicyclohexylammonium salt 
• 76003-54-8 Dicyclohexyl-amine; compound with phenyl-phosphonothioic acid O-ethyl ester 
• 6230-93-9 O-ethyl phenylphosphonothioic acid 
• 4546-19-4 ethyl hydrogen phenylphosphonate 
• 221616-26-8 (R)_P(+)-O,O-diethyl phosphoric O-ethyl phenylphosphonothioic anhydride 
• 5075-13-8 O-ethyl phenylphosphonochloridothioate 

Relevant articles and documents

A new hydrogen-bonding motif for chiral recognition in the diastereomeric salts of racemic 1-phenylethylamine derivatives with enantiopure O-ethyl phenylphosphonothioic acid

(Chemical Equation Presented) An enantiopure phosphonothioic acid showed a unique and superior chiral recognition ability, arising from its P-stereogenicity, for racemic 1-phenylethylamine derivatives through diastereomeric crystallization. Spherical molecular clusters, associated by hydrogen bonds and CH/π interactions, aggregated with high symmetry in the less-soluble diastereomeric salts.

Enantiopure O-substituted phenylphosphonothioic acids: Chiral recognition ability during salt crystallization and chiral recognition mechanism

The chiral recognition ability of enantiopure O-methyl, O-ethyl, O-propyl, and O-phenyl phenylphosphonothioic acids (1a-d) for various kinds of racemic amines during salt crystallization and the chiral recognition mechanism were thoroughly investigated. T