Fmoc-Cys(tert-butoxycarnylpropyl)-OH

Modify Date: 2024-01-02 12:26:00

Fmoc-Cys(tert-butoxycarnylpropyl)-OH Structure
Fmoc-Cys(tert-butoxycarnylpropyl)-OH structure
Common Name Fmoc-Cys(tert-butoxycarnylpropyl)-OH
CAS Number 102971-73-3 Molecular Weight 485.59200
Density N/A Boiling Point N/A
Molecular Formula C26H31NO6S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Fmoc-Cys(tert-butoxycarnylpropyl)-OH


N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(4-(tert-butoxy)-4-oxobutyl)-L-cysteine is a cysteine derivative[1].

 Names

Name 4-[(2R)-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethylsulfanyl]butyric acid tert butyl ester
Synonym More Synonyms

 Fmoc-Cys(tert-butoxycarnylpropyl)-OH Biological Activity

Description N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(4-(tert-butoxy)-4-oxobutyl)-L-cysteine 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

Molecular Formula C26H31NO6S
Molecular Weight 485.59200
Exact Mass 485.18700
PSA 127.23000
LogP 5.22430

 Synonyms

(R)-FMOC-2-AMINO-3-(3-TERT-BUTOXYCARBONYL-PROPYLSULFANYL)-PROPIONIC ACID
Fmoc-L-Cys(tert-butoxycarbonylpropyl)-OH
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