Top Suppliers:I want be here


129223-22-9

129223-22-9 structure
129223-22-9 structure
  • Name: Fmoc-Pro-Pro-OH
  • Chemical Name: (2S)-1-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid
  • CAS Number: 129223-22-9
  • Molecular Formula: C25H26N2O5
  • Molecular Weight: 434.484
  • Catalog: Biochemical Amino acids and their derivatives Proline derivatives
  • Create Date: 2018-06-30 17:41:25
  • Modify Date: 2024-01-09 20:45:34
  • Fmoc-Pro-Pro-OH is a proline derivative[1].

Name (2S)-1-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid
Synonyms 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-prolyl-L-proline
Fmoc-Pro-Pro-OH
1-{1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-prolyl}-L-prolin
N-Fmoc-L-prolyl-L-proline
L-Proline, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-prolyl-
Description Fmoc-Pro-Pro-OH is a proline 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 1.4±0.1 g/cm3
Boiling Point 677.7±55.0 °C at 760 mmHg
Molecular Formula C25H26N2O5
Molecular Weight 434.484
Flash Point 363.7±31.5 °C
Exact Mass 434.184174
PSA 87.15000
LogP 2.69
Appearance Solid
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.638
Storage condition -15°C
Hazard Codes Xi

~98%

129223-22-9 structure

129223-22-9

Literature: Dai, Zhi; Ye, Guozhong; Pittman Jr., Charles U.; Li, Tingyu Chirality, 2012 , vol. 24, # 4 p. 329 - 338

~75%

129223-22-9 structure

129223-22-9

Literature: Gayathri; Gopi; Suresh Babu Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1998 , vol. 37, # 2 p. 151 - 154

~%

129223-22-9 structure

129223-22-9

Literature: Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, , vol. 37, # 2 p. 151 - 154

~%

129223-22-9 structure

129223-22-9

Literature: Chirality, , vol. 24, # 4 p. 329 - 338

~%

129223-22-9 structure

129223-22-9

Literature: Chirality, , vol. 24, # 4 p. 329 - 338

~%

129223-22-9 structure

129223-22-9

Literature: Chirality, , vol. 24, # 4 p. 329 - 338