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n(alpha) n-(im)-di-boc-l-histidine

Names

[ CAS No. ]:
17791-51-4

[ Name ]:
n(alpha) n-(im)-di-boc-l-histidine

[Synonym ]:
N(|A),N-(im)-Di-Boc-L-histidine methyl ester
[Methyl(S)-3[1-(1,1-dimethylethoxycarbonyl)-1-H-imidazol-4-yl]-2-[(1,1-dimethylethoxycarbonyl)amino]propionate
methyl (S)-3-<1-(1,1-dimethylethoxycarbonyl)-1H-imidazol-5-yl>-2-<(1,1-dimethylethoxycarbonyl)amino>propionate
MFCD03094049

Biological Activity

[Description]:

N(α), N-(im)-Di-Boc-L-histidine methyl ester is a histidine derivative[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[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):1793-1144.

Chemical & Physical Properties

[ Density]:
1.17g/cm3

[ Melting Point ]:
113-116ºC(lit.)

[ Molecular Formula ]:
C17H27N3O6

[ Molecular Weight ]:
369.41300

[ Exact Mass ]:
369.19000

[ PSA ]:
112.24000

[ LogP ]:
2.47950

[ Index of Refraction ]:
1.516

[ Storage condition ]:
Store at 0-5°C

MSDS

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Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

Related Compounds