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N-Boc-trans-4-N-Fmoc-amino-L-proline

Names

[ CAS No. ]:
176486-63-8

[ Name ]:
N-Boc-trans-4-N-Fmoc-amino-L-proline

[Synonym ]:
(4R)-1-(tert-butoxycarbonyl)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-L-proline
N-BOC-TRANS-4-N-FMOC-AMINO-L-PROLINE
RARECHEM EM WB 0068
(4R)-4-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-1-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-proline
1,2-Pyrrolidinedicarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 1-(1,1-dimethylethyl) ester, (2S,4R)-
MFCD00673783

Biological Activity

[Description]:

(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is a proline 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]:
1.3±0.1 g/cm3

[ Boiling Point ]:
650.2±55.0 °C at 760 mmHg

[ Melting Point ]:
199ºC(lit.)

[ Molecular Formula ]:
C25H28N2O6

[ Molecular Weight ]:
452.500

[ Flash Point ]:
347.0±31.5 °C

[ Exact Mass ]:
452.194733

[ PSA ]:
105.17000

[ LogP ]:
3.86

[ Appearance of Characters ]:
Powder | White/off-white/palebrown

[ Vapour Pressure ]:
0.0±2.0 mmHg at 25°C

[ Index of Refraction ]:
1.627

[ 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

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
22

[ Safety Phrases ]:
36/37/38

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

Related Compounds