S-Phenyl-L-cysteine

Names

[ Name ]:
S-Phenyl-L-cysteine

[Synonym ]:
MFCD01318758
(2R)-2-amino-3-phenylthiopropanoic acid
S-phenyl-L-cysteine
L-Cysteine,S-phenyl
(L)-2-amino-3-(phenylthio)propanoic acid
(R)-S-Phenylcystein
Cysteine, S-phenyl-
S-Phenylcysteine
3-(Phenylthio)-L-Alanine,4-Thia-L-homophenylalanine
QVYZ1SR &&L or R Form
4-Thia-L-homophenylalanine
3-Phenylcysteine
L-S-phenylcysteine
(R)-S-phenylcysteine
S-Ph-L-cysteine
(R)-2-Amino-3-(phenylthio)propanoic acid
3-(Phenylthio)-L-Alanine

Biological Activity

[Description]:

S-Phenylcysteine is acysteine derivatives.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
361.5±37.0 °C at 760 mmHg

[ Melting Point ]:
200 °C (dec.)(lit.)

[ Molecular Formula ]:
C₉H₁₁NO₂S

[ Molecular Weight ]:
197.25

[ Flash Point ]:
172.4±26.5 °C

[ Exact Mass ]:
197.051056

[ PSA ]:
88.62000

[ LogP ]:
1.86

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.624

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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

Comparative study on the bioactivation mechanisms and cytotoxicity of Te-phenyl-L-tellurocysteine, Se-phenyl-L-selenocysteine, and S-phenyl-L-cysteine.

Chem. Res. Toxicol. 15(12) , 1610-8, (2002)

Tellurium compounds are effective antioxidants and chemoprotectors, even more active than their selenium and sulfur analogues. In addition to these properties, some selenium compounds, such as selenoc...

Biomarkers of human exposure to benzene.

J. Toxicol. Environ. Health A 40(2-3) , 377-86, (1993)

Three biomarkers for benzene exposure were developed. The first biomarker, muconic acid in urine, results from the ring opening of a benzene metabolite. A gas chromatography/mass spectroscopy (GC/MS) ...

S-phenylcysteine formation in hemoglobin as a biological exposure index to benzene.

Arch. Toxicol. 66(5) , 303-9, (1992)

Benzene is metabolized to intermediates that bind to hemoglobin, forming adducts. These hemoglobin adducts may be usable as biomarkers of exposure. In this paper, we describe the development of a gas ...