CAS 34317-61-8|S-Phenyl-L-cysteine

Introduction:Basic information about CAS 34317-61-8|S-Phenyl-L-cysteine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameS-Phenyl-L-cysteine
CAS Number34317-61-8Molecular Weight197.25
Density1.3±0.1 g/cm3Boiling Point361.5±37.0 °C at 760 mmHg
Molecular FormulaC9H11NO2SMelting Point200 °C (dec.)(lit.)
MSDSChineseUSAFlash Point172.4±26.5 °C

Names

Name(2R)-2-amino-3-phenylsulfanylpropanoic acid
SynonymMore Synonyms

S-Phenyl-L-cysteine BiologicalActivity

DescriptionS-Phenylcysteine is acysteine derivatives.
Related CatalogResearch Areas >>Others

Chemical & Physical Properties

Density1.3±0.1 g/cm3
Boiling Point361.5±37.0 °C at 760 mmHg
Melting Point200 °C (dec.)(lit.)
Molecular FormulaC9H11NO2S
Molecular Weight197.25
Flash Point172.4±26.5 °C
Exact Mass197.051056
PSA88.62000
LogP1.86
Vapour Pressure0.0±0.9 mmHg at 25°C
Index of Refraction1.624
InChIKeyXYUBQWNJDIAEES-QMMMGPOBSA-N
SMILESNC(CSc1ccccc1)C(=O)O

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi:Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS37/39-S26
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2930909090

Customs

HS Code2930909090
Summary2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles8

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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 ...

Synonyms

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
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