118629-70-2

Basic information

• Product Name: (S)-2-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate
• Synonyms: (S)-2-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate
• CAS NO: 118629-70-2
• Molecular Weight: 306.383
• Mol File: 118629-70-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (S)-2-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate(118629-70-2)
• EPA Substance Registry System: (S)-2-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate(118629-70-2)

Safety Data

• Hazardous Substances Data: 118629-70-2(Hazardous Substances Data)

Upstream product

• 20312-36-1 L-3-phenyllactic acid 
• 104-53-0 3-phenyl-propionaldehyde 
• 771476-48-3 (S)-3-phenyl-2-(N-phenyl-aminooxy)-propan-1-ol 
• 17131-14-5 (S)-(-)-3-phenyl-1,2-propanediol 
• 98-59-9 p-toluenesulfonyl chloride 
• 121958-41-6 [(2R,3R)-3-phenyloxiran-2-yl]methyl 4-methylbenzenesulfonate 
• 113826-06-5 (R)-glycidyl tosylate 
• 591-51-5 phenyllithium 

Downstream Products

• 91420-74-5 (S)-(2,3-epoxypropyl)benzene 
• 61393-94-0 (R)-2-benzyloxirane 

Relevant articles and documents

Synthesis of Seven-Membered Benzolactones by Nickel-Catalyzed C?H Coupling of Benzamides with Oxetanes

A NiCl2(PEt3)2-catalyzed regioselective C?H coupling of 8-aminoquinoline-derived benzamides with oxetanes has been developed. The reaction proceeds with concomitant removal of the 8-aminoquinoline auxiliary to directly for

NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS AND THE USES THEREOF

The invention relates to pyridinyl nicotinic acetylcholine receptor ligands, compositions comprising an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand and methods to treat or prevent a condition, such as depression and nicotine dependence, comprising administering to an animal in need thereof an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand.

Chemoselective reduction of 2,3-epoxy tosylates with DIBAL-H as a general route to enantiomerically-enriched 1-tosyloxy-2-alkanols

2,3-Epoxy tosylates may be reduced with DIBAL-H in CH2Cl2 or ether at -40°C to 1-tosyloxy-2-alkanols in high (94-98%) yields.