Fmoc-N-Me-D-Val-OH

Names

[ Name ]:
Fmoc-N-Me-D-Val-OH

[Synonym ]:
D-Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methylvaline
Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-methylbutanoic acid
MFCD00153396
Fmoc-N-Me-Val-OH
Fmoc-N-Me-D-Val-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-D-valine
(2R)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoic acid

Biological Activity

[Description]:

Fmoc-D-N-Me-Val-OH 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

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
527.6±29.0 °C at 760 mmHg

[ Molecular Formula ]:
C₂₁H₂₃NO₄

[ Molecular Weight ]:
353.412

[ Flash Point ]:
272.9±24.3 °C

[ Exact Mass ]:
353.162720

[ PSA ]:
66.84000

[ LogP ]:
4.91

[ Vapour Pressure ]:
0.0±1.5 mmHg at 25°C

[ Index of Refraction ]:
1.588

[ Storage condition ]:
2-8°C

Safety Information

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
22-24/25

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%