28713-50-0

Basic information

• Product Name: Benzenemethanol, a-(mercaptomethyl)-
• Synonyms: 2-hydroxy-2-phenylethanethiol;2-mercapto-1-phenethyl alcohol;2-Mercapto-1-phenyl-ethanol;2-mercapto-1-phenylethanol;mercapto-2 phenyl-1 ethanol-1;1-phenyl-2-mercaptoethanol
• CAS NO: 28713-50-0
• Molecular Formula: C8H10OS
• Molecular Weight: 154.233
• Mol File: 28713-50-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 84 - 87 °C (1 - 1.5 mmHg)
• CAS DataBase Reference: Benzenemethanol, a-(mercaptomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(mercaptomethyl)-(28713-50-0)
• EPA Substance Registry System: Benzenemethanol, a-(mercaptomethyl)-(28713-50-0)

Safety Data

• Hazardous Substances Data: 28713-50-0(Hazardous Substances Data)

Upstream product

• 2984-50-1 1,2-Epoxyoctane 
• 98-86-2 acetophenone 
• 100-52-7 benzaldehyde 
• 100-42-5 styrene 
• 96-09-3 styrene oxide 
• 3385-94-2 hexamethyldisilathiane 
• 53392-49-7 phenacyl thioacetate 
• 3101-60-8 4-tert-butylphenyl 2,3-epoxypropyl ether 
• 98194-92-4 1-Phenyl-2-(tetrahydro-pyran-2-ylsulfanyl)-ethanol 
• 70-11-1 α-bromoacetophenone 
• 85260-02-2 2-(2-Oxo-2-phenyl-ethylsulfanyl)-isoindole-1,3-dione 
• 1539-42-0 bis[(2-pyridyl)methyl]amine 
• 105247-56-1 dithiobenzoate d'hydroxy-2 phenyl-2 ethyle 
• 133386-58-0 dithiocarbonic acid O-benzyl ester-S-phenacyl ester 

Downstream Products

• 98204-52-5 2-phenyl-1-oxa-4-thia-spiro[4.5]decane 
• 119119-66-3 1-phenyl-2-(vinylthio)ethanol 
• 119119-69-6 cis-3-phenyl-1,4-oxathiane S-oxide 
• 119119-69-6 trans-3-phenyl-1,4-oxathiane S-oxide 
• 119119-67-4 R*,R*-1-phenyl-2-(vinylthio)ethanol 
• 119119-67-4 R*,S*-1-phenyl-2-(vinylthio)ethanol 
• 23451-56-1 2-(ethylthio)-1-phenylethanol 

Relevant articles and documents

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A new strategy for chemoselective O-acylation of β-mercapto alcohols via alkylsilyl and stannyl protection

Chemoselective preparation of O-acylated derivatives from bis-protected mercapto alcohols was described. Trialkylsilyl and trialkylstannyl chloride are used to generate an intermediate with O- and S-protection. The intermediates from β-mercapto alcohols a

Synthesis of thiols via palladium catalyzed methanolysis of thioacetates with borohydride exchange resin

Various thiols are prepared quantitatively from the corresponding thioacetates via Pd catalyzed methanolysis with borohydride exchange resin under a mild and neutral conditions. One-pot synthesis of thiols from alkyl halides through the formation of alkyl thioacetates using thioacetate exchange resin followed by methanolysis is also described.