Val-OBzl HCl

Names

[ Name ]:
Val-OBzl HCl

[Synonym ]:
H-Val-OBn HCl
Benzyl L-valinate hydrochloride (1:1)
Val-OBzl HCl
2-Butanaminium, 3-methyl-1-oxo-1-(phenylmethoxy)-, chloride, (2S)- (1:1)
MFCD00058010
H-Val-OBzl.HCl
H-L-Val-OBn*HCl
valine benzyl ester hydrochloride
L-Valine Benzyl Ester Hydrochloride
(2S)-1-(Benzyloxy)-3-methyl-1-oxo-2-butanaminium chloride
H-Val-OBzl·HCl
L-valine, phenylmethyl ester, hydrochloride (1:1)
L-Valine benzylester hydrochloride

Biological Activity

[Description]:

H-Val-Obzl.HCl is a valine 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

[ Boiling Point ]:
285.5ºC at 760 mmHg

[ Melting Point ]:
138 °C

[ Molecular Formula ]:
C₁₂H₁₈ClNO₂

[ Molecular Weight ]:
243.730

[ Flash Point ]:
143.7ºC

[ Exact Mass ]:
243.102600

[ PSA ]:
52.32000

[ LogP ]:
3.21540

[ Vapour Pressure ]:
0.0028mmHg at 25°C

[ Index of Refraction ]:
-10 ° (C=2, H2O)

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Precursor & DownStream

Precursor

DownStream

Articles

Synthesis of 7-substituted benzolactam-V8s and their selectivity for protein kinase C isozymes.

Org. Lett. 4 , 2377-2380, (2002)

[reaction: see text] Condensation of L-valine benzyl ester toluenesulfonic acid salt with a substituted cyclohexadione followed by aromatization with the assistance of NBS provides an N-aryl L-valine ...