63067-91-4

Basic information

• Product Name: 2-Propen-1-ol, 2-(phenylsulfinyl)-
• CAS NO: 63067-91-4
• Molecular Formula: C9H10O2S
• Molecular Weight: 182.243
• Mol File: 63067-91-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-ol, 2-(phenylsulfinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-ol, 2-(phenylsulfinyl)-(63067-91-4)
• EPA Substance Registry System: 2-Propen-1-ol, 2-(phenylsulfinyl)-(63067-91-4)

Safety Data

• Hazardous Substances Data: 63067-91-4(Hazardous Substances Data)

Upstream product

• 74338-92-4 3-bromo-2-phenylsulphinylyprop-1-ene 
• 74338-75-3 2-cyanoethyl(phenyl)sulfoxide 
• 106-96-7 propargyl bromide 
• 127-09-3 sodium acetate 
• 90838-29-2 3-chloro-2-(phenylsulfinyl)-1-propene 
• 52072-15-8 2-(phenylthio)-2-propenyl alcohol 
• 50-00-0 formaldehyd 
• 50746-65-1 Diethyl (phenylsulfinyl)methylphosphonate 
• 108-98-5 thiophenol 
• 3055-87-6 3-(phenylthio)propionitrile 
• 371764-76-0 acetic acid 2-benzenesulfinyl-allyl ester 
• 107-19-7 propargyl alcohol 

Downstream Products

• 123533-83-5 N-p-tolyl-3-ethoxycarbonyl-5-phenylsulphinyl-3,4,5,6-tetrahydro-2(1H)-pyridone 
• 123533-76-6 N-p-tolyl-N-(2-phenylsulphinylprop-2-enyl)amine 
• 74338-92-4 3-bromo-2-phenylsulphinylyprop-1-ene 
• 245556-58-5 2-phenylsulphinyl-3-methanesulphonyloxyprop-1-ene 
• 123533-73-3 2-phenylsulphinyl-3-p-toluenesulphonyloxyprop-1-ene 

Relevant articles and documents

First synthesis of (±)-pseudohygrophorone A12, an anti-fungal cyclohexenone derivative isolated from Hygrophorus abieticola

Pseudohygrophorones A12 and B12 are cyclohexenone derivatives isolated from Hygrophorus abieticola (Basidiomycete) as anti-phytopathogenic compounds. In this study, the first synthesis of (±)-pseudohygrophorones A12 is rep

Reagents for rapid peptide synthesis

This invention relates to compounds of the formula: STR1 wherein R is an electron withdrawing group; R1 is H or COZ; X1 and X2 are independently H, lower alkyl, aryl, aryl lower-alkyl or polystyrene or R and X1 taken together with the carbon atoms to which they are attached form a ring containing from 4 to 15 ring carbon atoms and may contain up to 2 heteroatoms, wherein the heteroatoms are O, S, or N; and Z is an amino acid residue, a peptide residue or a leaving group. The compounds of the present invention are adaptable as blocking or protecting groups for an amine composition useful in peptide synthesis. The present invention is also directed to a method of protecting an amino group of an organic molecule during a reaction which modifies a portion of the molecule other than the protected amino group.