1116119-83-5

Basic information

• Product Name: (2S,3S)-3-phenylthio-1,2,3,4-tetrahydro-2-naphthalenol
• Synonyms: (2S,3S)-3-phenylthio-1,2,3,4-tetrahydro-2-naphthalenol
• CAS NO: 1116119-83-5
• Molecular Weight: 256.368
• Mol File: 1116119-83-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2S,3S)-3-phenylthio-1,2,3,4-tetrahydro-2-naphthalenol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-3-phenylthio-1,2,3,4-tetrahydro-2-naphthalenol(1116119-83-5)
• EPA Substance Registry System: (2S,3S)-3-phenylthio-1,2,3,4-tetrahydro-2-naphthalenol(1116119-83-5)

Safety Data

• Hazardous Substances Data: 1116119-83-5(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 2461-35-0 2,3-epoxy-1,2,3,4-tetrahydronaphthalene 
• 108-98-5 thiophenol 
• 2461-35-0 2,3-epoxy-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Lithium BINOL phosphate catalyzed desymmetrization of meso-epoxides with aromatic thiols

A highly enantioselective method for desymmetrization of meso-epoxides using thiols is reported. This is the first example of epoxide activation achieved using metal BINOL phosphates. The reaction has a broad scope in terms of epoxide substrates and aroma

Catalytic asymmetric ring-opening reaction of meso-epoxides with aryl selenols and thiols catalyzed by a heterobimetallic gallium-titanium-salen complex

A chiral heterobimetallic Lewis acid complex has been developed as an efficient catalyst. The enantioselective desymmetrization of meso-epoxides with aryl selenols and thiols catalyzed by the heterobimetallic complex has been optimized. The optically active β-arylseleno alcohols and β-hydroxy sulfides were obtained in good yields and high enantioselec- tivities (up to 97% ee and 92% ee, respectively). A strong synergistic effect between different Lewis acids was exhibited in the catalytic process. & copy; 2009 Wiley-VCH Verlag GmbH & Co. KGaA.