5149-48-4

Basic information

• Product Name: 3-(Phenylthio)-1,2-propanediol
• Synonyms: 3-(Phenylthio)-1,2-propanediol
• CAS NO: 5149-48-4
• Molecular Formula: C₉H₁₂O₂S
• Molecular Weight: 184.2554
• Mol File: 5149-48-4.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 369.2°Cat760mmHg
• Flash Point: 179.5°C
• Appearance: /
• Density: 1.23g/cm³
• Vapor Pressure: 4.21E-06mmHg at 25°C
• Refractive Index: 1.609
• CAS DataBase Reference: 3-(Phenylthio)-1,2-propanediol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Phenylthio)-1,2-propanediol(5149-48-4)
• EPA Substance Registry System: 3-(Phenylthio)-1,2-propanediol(5149-48-4)

Safety Data

• Hazardous Substances Data: 5149-48-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H12O2S/c10-6-8(11)7-12-9-4-2-1-3-5-9/h1-5,8,10-11H,6-7H2

Upstream product

• 108-98-5 thiophenol 
• 96-24-2 3-monochloro-1,2-propanediol 
• 930-69-8 sodium thiophenolate 
• 5296-21-9 2-(phenylsulfanylmethyl)oxirane 
• 584-07-6 methyl N-hydroxycarbamate 
• 13318-11-1 2-((4-nitrobenzoyloxy)methyl)oxirane 
• 3111-52-2 potassium thiophenolate 
• 96426-73-2 Glycidyl N,N-dimethylcarbamate 
• 110210-93-0 2-hydroxy-3-phenylthiopropyl acetate 
• 14007-09-1 2-(2-methoxyphenoxy)-1,3-propanediol 
• 93-14-1 guaifenesin 
• 5296-64-0 allyl phenyl thioether 
• 4704-77-2 1-bromo-2,3-propanediol 
• 556-52-5 oxiranyl-methanol 

Downstream Products

• 27098-65-3 3-phenylsulfanyl-propionaldehyde 
• 66303-55-7 2-(phenylthio)acetaldehyde 
• 5149-50-8 Benzenesulfinyl-acetaldehyde 
• 143945-89-5 3-benzenesulfonyl-propane-1,2-diol 
• 38513-17-6 1-Phenylsulfonyl-3-prop-1-enyl-methansulfonat 
• 111248-45-4 2-(phenylthio)acetaldehyde cyanohydrin 
• 111248-38-5 phenylthioacetaldehyde cyanohydrin acetate 

Relevant articles and documents

One-pot catalyst-free synthesis of β-and γ-hydroxy sulfides using diaryliodonium salts and microwave irradiation

A simple and rapid one-pot protocol is described for the preparation of α- and β-hydroxy sulfides. The direct solvent-free microwave irradiation of diaryliodonium salts, potassium thiocyanate, and ethylene glycol/β-propylene glycol without any catalyst or base affords the final compounds in good yields (65-95 %) in around 10-25 min. Copyright

Method for the dihydroxylation of olefins using transition metal catalysts

This invention relates to process for dihydroxylation of olefins using transition metal catalysts to obtain monofunctional, bifunctional, and/or polyfunctional 1,2-diols of the formula (I) R1R2C(OH)—C(OH)R3R4??(I) where R1to R4are defined herein, by reacting an olefin of the formula (II) R1R2C═CR3R4??(II) where R1to R4are defined as for formula (I), with molecular oxygen in the presence of an osmium, ruthenium, or manganese compound in water or a water-containing solvent mixture at a pH of from 7.5 to 13.

Naphthyloxy acetic acid derivatives and a pharmaceutical composition comprising them as an active ingredient

The naphthyloxyacetic acid derivatives of the formula (I) wherein A is H, -(alkylene)COOR1, -(alkylene)CONR2R3, -(alkylene)OH, -(alkylene)tetrazole, -(alkylene)CN; E is single bond or alkylene; G is —S—, —SO—, —SO2—, —O— or —NR4—; L is alkylene, —(CH2)m—CH═CH—(CH2)n— or —(CH2)x—CH(OH)—(CH2)y—; M is phenyl, phenyl(thio, oxy, amino), diphenylmethyl, diphenylmethyl(thio, oxy, amino), and pharmaceutical composition comprising them as an active ingradient. The compounds of the formula (I) can combine PGE2receptor and exhibit the activity to antagonize or agonize for PGE2receptor. Therefore, they are useful as anti-hyperlipemia, for the prevention of abortion, for analgesics, as antidiarrheals, sleep inducer, diuretic, anti-diabetes, abortient, cathartics, antiulcer, anti-gastritis or antihypertensive etc.