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5068-28-0

5068-28-0 structure
5068-28-0 structure

Name Boc-S-Benzyl-L-cysteine
Synonyms Boc-Cys(Bzl)-OH
N-Boc-S-Benzyl-L-Cys-OH
N-Boc-S-benzyl-L-cysteine
L-Cysteine, N-((1,1-dimethylethoxy)carbonyl)-S-(phenylmethyl)-
Boc-S-Benzyl-L-Cysteine
N-tert-butoxycarbonyl-S-benzylcysteine
N-α-t-Boc-S-benzyl-L-cysteine
N-(tert-Butoxycarbonyl)-S-benzyl-L-cysteine
BOC-S-BENZYL-CYSTEINE
(R)-3-(Benzylthio)-2-((tert-butoxycarbonyl)amino)propanoic acid
t-butyloxycarbonyl-S-benzyl-L-cysteine
EINECS 225-772-8
MFCD00065567
S-Benzyl-N-(tert-butoxycarbonyl)-L-cysteine
S-benzyl N-Boc-cysteine
S-Benzyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-cysteine
L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(phenylmethyl)-
Description (R)-3-(Benzylthio)-2-((tert-butoxycarbonyl)amino)propanoic acid 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.

Density 1.2±0.1 g/cm3
Boiling Point 481.2±45.0 °C at 760 mmHg
Melting Point 86-88 °C
Molecular Formula C15H21NO4S
Molecular Weight 311.397
Flash Point 244.8±28.7 °C
Exact Mass 311.119141
PSA 100.93000
LogP 3.93
Vapour Pressure 0.0±1.3 mmHg at 25°C
Index of Refraction 1.554
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090

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5068-28-0 structure

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Literature: Koerber-Ple; Massiot Journal of Heterocyclic Chemistry, 1995 , vol. 32, # 4 p. 1309 - 1315

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Literature: Koerber-Ple; Massiot Journal of Heterocyclic Chemistry, 1995 , vol. 32, # 4 p. 1309 - 1315

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Literature: Anderson; McGregor Journal of the American Chemical Society, 1957 , vol. 79, p. 6180,6181

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Literature: AXYS PHARMACEUTICALS, INC. Patent: WO2004/838 A1, 2003 ; Location in patent: Page 85 ; WO 2004/000838 A1

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Literature: Richter, Lutz S.; Marsters Jr., James C.; Gadek, Thomas R. Tetrahedron Letters, 1994 , vol. 35, # 11 p. 1631 - 1634

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Literature: Khan,S.A.; Sivanandaiah,K.M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1977 , vol. 15, p. 80 - 81

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Literature: Itoh,M. et al. Bulletin of the Chemical Society of Japan, 1977 , vol. 50, p. 718 - 721

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5068-28-0

Literature: Broadbent,W. et al. Journal of the Chemical Society [Section] C: Organic, 1967 , p. 2632 - 2636

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Literature: Ageeva; Kurzeev; Kazankov Russian Journal of Organic Chemistry, 2007 , vol. 43, # 4 p. 548 - 552
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%