phenylethylthiol

Suppliers

Names

[ CAS No. ]:
622-38-8

[ Name ]:
phenylethylthiol

[Synonym ]:
Benzene, (ethylthio)-
phenylethylthiol
Phenylethyl sulfide
(1-Thiapropyl)benzene
(Phenylthio)ethane
Sulfide, ethyl phenyl (8CI)
Ethyl phenyl sulfide
Sulfide, ethyl phenyl
EINECS 210-731-9
Phenyl ethyl sulfide
ethylsulfanylbenzene
MFCD00009265
(Ethylsulfanyl)benzene

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
202.9±9.0 °C at 760 mmHg

[ Molecular Formula ]:
C8H10S

[ Molecular Weight ]:
138.230

[ Flash Point ]:
73.9±0.0 °C

[ Exact Mass ]:
138.050323

[ PSA ]:
25.30000

[ LogP ]:
3.24

[ Vapour Pressure ]:
0.4±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.557

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Bromoethane
  • Diphenyl disulfide
  • Ethyl iodide
  • Iodobenzene
  • Ethanethiol
  • ethyl acetate
  • Thiophenol
  • Ethyl carbonate
  • Diethyl ether

DownStream

  • 2-ethylsulfanylbenzoic acid
  • benzoic acid
  • ethene
  • Diphenylsulfid
  • P-toluenethiol
  • Phenyl phenylthio sulfone
  • Ethyl phenyl sulfone
  • Diphenyldisulfon
  • 1-chloroethylsulfinylbenzene

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Mechanism of sulfide oxidations by peroxymonocarbonate.

Inorg. Chem. 40(13) , 2996-3001, (2001)

A detailed mechanism for the oxidation of aryl sulfides by peroxymonocarbonate ion in cosolvent/water media is described. Kinetic studies were performed to characterize the transition state, including...


More Articles

Related Compounds

  • 2-(3,4-dimethoxyphenyl)-4-methyl-N-[(2E)-5-(2-methylpropyl)-1,3,4-thiadiazol-2(3H)-ylidene]-1,3-thiazole-5-carboxamide
  • 1-(6-chloropyridazin-3-yl)-N-(4-methyl-1,3-thiazol-2-yl)piperidine-4-carboxamide
  • (5-methyl-1-phenyl-1H-pyrazol-4-yl)(3-(3-(pyridin-4-yl)-1,2,4-oxadiazol-5-yl)azetidin-1-yl)methanone
  • 5-bromo-N-(3-methylisothiazol-5-yl)furan-2-carboxamide
  • 4-amino-3-(2,5-dimethylphenyl)-N-(4-methylbenzyl)-2-thioxo-2,3-dihydrothiazole-5-carboxamide
  • 4-amino-N-cyclopentyl-3-(2,5-dimethylphenyl)-2-thioxo-2,3-dihydrothiazole-5-carboxamide
  • methyl 3-(4-amino-5-(azepane-1-carbonyl)-2-thioxothiazol-3(2H)-yl)benzoate
  • 2-(5-amino-3-(phenylamino)-4-tosyl-1H-pyrazol-1-yl)-N-(4-methylbenzyl)acetamide
  • [5-methyl-2-(4-methylphenyl)-1,3-oxazol-4-yl]methyl 1-(4-chlorophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxylate
  • [2-(4-ethoxyphenyl)-5-methyl-1,3-oxazol-4-yl]methyl 1-(4-chlorophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxylate
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.