14156-07-1

Basic information

• Product Name: O,O′-diphenyl S-hydrogen phosphorothioate
• Synonyms: O,O′-diphenyl S-hydrogen phosphorothioate
• CAS NO: 14156-07-1
• Molecular Weight: 266.257
• Mol File: 14156-07-1.mol

Chemical Properties

• CAS DataBase Reference: O,O′-diphenyl S-hydrogen phosphorothioate(CAS DataBase Reference)
• NIST Chemistry Reference: O,O′-diphenyl S-hydrogen phosphorothioate(14156-07-1)
• EPA Substance Registry System: O,O′-diphenyl S-hydrogen phosphorothioate(14156-07-1)

Safety Data

• Hazardous Substances Data: 14156-07-1(Hazardous Substances Data)

Upstream product

• 597-82-0 O,O,O-triphenyl phosphorothioate 
• 75-15-0 carbon disulfide 
• 4712-55-4 diphenyl hydrogen phosphite 
• 80141-24-8 Phosphorigsaeure-diphenyl-trimethylsilylester 
• 108-95-2 phenol 
• 110-80-5 2-ethoxy-ethanol 
• 66055-41-2 O,O-diphenyl O-n-propyl phosphorothionate 
• 22077-44-7 O,O-diphenyl phosphorochloridothioate 

Downstream Products

• 30342-92-8 2-phenoxy-2-oxo-1,3,2-oxathiaphosphorinane 
• 108-95-2 phenol 
• 65190-56-9 Thiophosphoric acid S-benzhydryl ester O,O'-diphenyl ester 
• 22077-44-7 O,O-diphenyl phosphorochloridothioate 
• 16749-41-0 5,6-Didesoxy-5,6-epithio-1,2-O-isopropyliden-α-L-idofuranose 
• 838-85-7 diphenyl hydrogen phosphate 
• 103950-07-8 (3aR,5S,6S,6aR)-2,2-Dimethyl-5-((S)-2-oxo-2-phenoxy-2λ⁵-[1,3,2]oxathiaphospholan-5-yl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 103950-09-0 Thiophosphoric acid S-[(S)-2-hydroxy-2-((3aR,5S,6S,6aR)-6-hydroxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl] ester O,O'-diphenyl ester 
• 87763-58-4 tetraphenyl thiopyrophosphate 
• 1212-29-9 1,3-dicyclohexylthiourea 
• 81017-64-3 N-(diphenoxyphosphoryl)-N,N'-dicyclohexylthiourea 

Relevant articles and documents

Bifunctional Thiourea-Catalyzed Stereoablative Retro-Sulfa-Michael Reaction: Concise and Diastereoselective Access to Chiral 2,4-Diarylthietanes

Owing to the chiral recognition capacity of bifunctional thioureas, a stereoablative retro-sulfa-Michael reaction has been developed. Utilization of a biphasic system enabled us to render the process catalytic. The usefulness of this methodology was further illustrated by the diastereoselective synthesis of all possible stereoisomers of 2,4-diarylthiethanes.

On the sulfurization of h-phosphonate diesters and phosphite triesters using elemental sulfur

Sulfurization of tetracoordinate and tricoordinate P(III) derivatives, namely, H-phosphonate diesters, H-phosphonothioate diesters, and phosphite triesters with elemental sulfur under various experimental conditions, was investigated.

Synthesis of methylene bisphosphonates from carbon disulfide and phosphites via desulfurization: A mechanistic study

The reaction of carbon disulfide with an excess of sodium dialkylphosphite in an aprotic solvent led to the formation of the carbanion of methylene bisphosphonate and sodium thiophosphate. The mechanistic study of this unexpected reaction, using both 31P