S-Phenyl-L-cysteine structure
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Common Name | S-Phenyl-L-cysteine | ||
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CAS Number | 34317-61-8 | Molecular Weight | 197.25 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 361.5±37.0 °C at 760 mmHg | |
Molecular Formula | C9H11NO2S | Melting Point | 200 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | 172.4±26.5 °C |
Use of S-Phenyl-L-cysteineS-Phenylcysteine is acysteine derivatives. |
Name | (2R)-2-amino-3-phenylsulfanylpropanoic acid |
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Synonym | More Synonyms |
Description | S-Phenylcysteine is acysteine derivatives. |
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Related Catalog |
Density | 1.3±0.1 g/cm3 |
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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 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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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 |
Precursor 9 | |
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DownStream 7 | |
HS Code | 2930909090 |
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Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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... |
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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) ... |
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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 ... |
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 |