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152548-66-8

152548-66-8 structure
152548-66-8 structure

Name Fmoc-N-Me-Asp(OtBu)-OH
Synonyms MFCD00237027
Fmoc-N-methyl-L-aspartic acid 4-tert-butyl ester
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-, 4-(1,1-dimethylethyl) ester
N-Methyl aspartic acid
(2S)-4-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)amino}-4-oxobutanoic acid (non-preferred name)
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl](methyl)amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid
Description Fmoc-N-Me-Asp(OtBu)-OH is an aspartic acid 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):1793-1144.

Density 1.2±0.1 g/cm3
Boiling Point 598.7±50.0 °C at 760 mmHg
Melting Point 135-140°C
Molecular Formula C24H27NO6
Molecular Weight 425.474
Flash Point 315.9±30.1 °C
Exact Mass 425.183838
PSA 93.14000
LogP 5.65
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.575
Storage condition -15°C
Symbol GHS09
GHS09
Signal Word Warning
Hazard Statements H410
Precautionary Statements P273-P501
Hazard Codes N
Risk Phrases 50/53
Safety Phrases 60-61
RIDADR UN 3077 9 / PGIII
Precursor  3

DownStream  0