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Boc-β-HomoThr(Bzl)-OH

Names

[ CAS No. ]:
254101-11-6

[ Name ]:
Boc-β-HomoThr(Bzl)-OH

[Synonym ]:
4-O-Benzyl-2,3,5-trideoxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-D-threo-pentonic acid
Boc-beta-Homothr(Bzl)-OH
(3R,4R)-4-(benzyloxy)-3-{[(tert-butoxy)carbonyl]amino}pentanoic acid
Boc-b-HoThr(Bzl)-OH
BOC-THR(OBZL)-(C*CH2)OH
Boc-β-HomoThr(Bzl)-OH

Biological Activity

[Description]:

(3R,4R)-4-(benzyloxy)-3-((tert-butoxycarbonyl)amino)pentanoic acid is a threonine 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]:
1.135g/cm3

[ Boiling Point ]:
485.4ºC at 760mmHg

[ Molecular Formula ]:
C17H25NO5

[ Molecular Weight ]:
323.38400

[ Flash Point ]:
247.4ºC

[ Exact Mass ]:
323.17300

[ PSA ]:
84.86000

[ LogP ]:
3.35060

[ Vapour Pressure ]:
3.1E-10mmHg at 25°C

[ Index of Refraction ]:
1.516

Safety Information

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

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Related Compounds