Fmoc-3,4-dehydro-L-proline

Names

[ Name ]:
Fmoc-3,4-dehydro-L-proline

[Synonym ]:
(2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2,5-dihydro-1H-pyrrole-2-carboxylic acid
1H-Pyrrole-1,2-dicarboxylic acid, 2,5-dihydro-, 1-(9H-fluoren-9-ylmethyl) ester, (2S)-
(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)-2,5-dihydropyrrole-2-carboxylic acid

Biological Activity

[Description]:

(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,5-dihydro-1H-pyrrole-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]:
1.4±0.1 g/cm3

[ Boiling Point ]:
549.6±50.0 °C at 760 mmHg

[ Molecular Formula ]:
C₂₀H₁₇NO₄

[ Molecular Weight ]:
335.353

[ Flash Point ]:
286.2±30.1 °C

[ Exact Mass ]:
335.115753

[ PSA ]:
66.84000

[ LogP ]:
2.97

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.653

[ Storage condition ]:
-15°C

Fmoc-3,4-dehydro-L-proline

Names

Biological Activity

Chemical & Physical Properties

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Related Compounds