H-Cys(Bzl)-OH

Modify Date: 2024-01-02 19:57:52

H-Cys(Bzl)-OH Structure
H-Cys(Bzl)-OH structure
 Common Name H-Cys(Bzl)-OH
CAS Number 3054-01-1 Molecular Weight 211.281
Density 1.3±0.1 g/cm3 Boiling Point 379.2±42.0 °C at 760 mmHg
Molecular Formula C10H13NO2S Melting Point 209-214ºC
MSDS Chinese USA Flash Point 183.2±27.9 °C

 Use of H-Cys(Bzl)-OH


H-Cys(Bzl)-OH is a cysteine derivative[1].

 Names

Name (R)-S-Benzylcysteine
Synonym More Synonyms

 H-Cys(Bzl)-OH Biological Activity

Description H-Cys(Bzl)-OH is a cysteine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-807.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 379.2±42.0 °C at 760 mmHg
Melting Point 209-214ºC
Molecular Formula C10H13NO2S
Molecular Weight 211.281
Flash Point 183.2±27.9 °C
Exact Mass 211.066696
PSA 88.62000
LogP 2.10
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.609

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090

 Synthetic Route

 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%

 Articles19

More Articles
Comparison of peak-picking workflows for untargeted liquid chromatography/high-resolution mass spectrometry metabolomics data analysis.

Rapid Commun. Mass Spectrom. 29(1) , 119-27, (2014)

Data analysis is a key step in mass spectrometry based untargeted metabolomics, starting with the generation of generic peak lists from raw liquid chromatography/mass spectrometry (LC/MS) data. Due to...

Formation of a dehydroalanyl residue from S-benzylcysteine upon HF cleavage of a [Sar1, Cys8]-angiotensin II peptide resin.

Int. J. Pept. Protein Res. 38(6) , 601-2, (1991)

Synthesis and biological evaluation of L-cysteine derivatives as mitotic kinesin Eg5 inhibitors.

Bioorg. Med. Chem. Lett. 17 , 3921-4, (2007)

Inhibition of Eg5 represents a novel approach for the treatment of cancer. Here, we report the synthesis and structure-activity relationship of S-trityl-L-cysteine (STLC) derivatives as Eg5 inhibitors...

 Synonyms

Alanine, 3- (benzylthio)-, L-
D-S-Benzylcysteine
EINECS 221-273-4
MFCD00002613
H-CYS(BZL)-OH
H-L-CYS(BZL)-OH
S-Benzyl-L-Cysteine
Benzylcysteine
(L)-2-amino-3-(benzylthio)propanoic acid
(S)-BENZYL-L-CYS
(S)-S-benzylcysteine
L-Cysteine, S- (phenylmethyl)-
L-S-benzylcysteine
(R)-2-Amino-3- (S-Benzylthio)Propanoic Acid
S-Benzylcysteine
BENZYL-S-CYSTEINE
(R)-2-Amino-3-(benzylthio)propanoic acid
Cysteine, S-(phenylmethyl)-
S-Bzl-L-Cys
CYSTEINE(BZL)-OH
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