Boc-Cys(Bzl)-OH

Modify Date: 2024-01-03 19:14:39

Boc-Cys(Bzl)-OH Structure
Boc-Cys(Bzl)-OH structure
Common Name Boc-Cys(Bzl)-OH
CAS Number 5068-28-0 Molecular Weight 311.397
Density 1.2±0.1 g/cm3 Boiling Point 481.2±45.0 °C at 760 mmHg
Molecular Formula C15H21NO4S Melting Point 86-88 °C
MSDS Chinese USA Flash Point 244.8±28.7 °C

 Use of Boc-Cys(Bzl)-OH


(R)-3-(Benzylthio)-2-((tert-butoxycarbonyl)amino)propanoic acid is a cysteine derivative[1].

 Names

Name Boc-S-Benzyl-L-cysteine
Synonym More Synonyms

 Boc-Cys(Bzl)-OH Biological Activity

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.

 Chemical & Physical Properties

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

 Safety Information

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

 Synthetic Route

~99%

Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

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Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

~%

Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

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Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

~%

Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

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Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

~%

Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

~%

Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

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Boc-Cys(Bzl)-OH Structure

Boc-Cys(Bzl)-OH

CAS#:5068-28-0

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

 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%

 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)-
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