![]() Fmoc-D-Phe-OH structure
|
Common Name | Fmoc-D-Phe-OH | ||
---|---|---|---|---|
CAS Number | 86123-10-6 | Molecular Weight | 387.428 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 620.1±50.0 °C at 760 mmHg | |
Molecular Formula | C24H21NO4 | Melting Point | 181-185ºC | |
MSDS | Chinese USA | Flash Point | 328.8±30.1 °C |
Use of Fmoc-D-Phe-OHFmoc-D-Phe-OH is a phenylalanine derivative[1]. |
Name | (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoic acid |
---|---|
Synonym | More Synonyms |
Description | Fmoc-D-Phe-OH is a phenylalanine 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 |
Density | 1.3±0.1 g/cm3 |
---|---|
Boiling Point | 620.1±50.0 °C at 760 mmHg |
Melting Point | 181-185ºC |
Molecular Formula | C24H21NO4 |
Molecular Weight | 387.428 |
Flash Point | 328.8±30.1 °C |
Exact Mass | 387.147064 |
PSA | 75.63000 |
LogP | 5.41 |
Vapour Pressure | 0.0±1.9 mmHg at 25°C |
Index of Refraction | 1.633 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
---|---|
Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2924299090 |
~86% Fmoc-D-Phe-OH CAS#:86123-10-6 |
Literature: Taber, Douglass F.; Berry, James F.; Martin, Timothy J. Journal of Organic Chemistry, 2008 , vol. 73, # 23 p. 9334 - 9339 |
~67% Fmoc-D-Phe-OH CAS#:86123-10-6 |
Literature: Huhtiniemi, Tero; Salo, Heikki S.; Suuronen, Tiina; Poso, Antti; Salminen, Antero; Leppaenen, Jukka; Jarho, Elina; Lahtela-Kakkonen, Maija Journal of Medicinal Chemistry, 2011 , vol. 54, # 19 p. 6456 - 6468 |
~95% Fmoc-D-Phe-OH CAS#:86123-10-6 |
Literature: Djedaini-Pilard, Florence; Azaroual-Bellanger, Nathalie; Gosnat, Muriel; Vernet, Delphine; Perly, Bruno Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1995 , # 4 p. 723 - 730 |
~% Fmoc-D-Phe-OH CAS#:86123-10-6 |
Literature: Journal of the American Chemical Society, , vol. 119, # 4 p. 656 - 673 |
~% Fmoc-D-Phe-OH CAS#:86123-10-6 |
Literature: Journal of the American Chemical Society, , vol. 117, # 32 p. 8488 - 8489 |
Precursor 4 | |
---|---|
DownStream 6 | |
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% |
1,4-disubstituted-[1,2,3]triazolyl-containing analogues of MT-II: design, synthesis, conformational analysis, and biological activity.
J. Med. Chem. 57(22) , 9424-34, (2014) Side chain-to-side chain cyclizations represent a strategy to select a family of bioactive conformations by reducing the entropy and enhancing the stabilization of functional ligand-induced receptor c... |
|
Solid-phase synthesis of C-terminal azapeptides.
J. Pept. Sci. 21 , 387-91, (2015) The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated ... |
|
Preclinical evaluation of a high-affinity 18F-trifluoroborate octreotate derivative for somatostatin receptor imaging.
J. Nucl. Med. 55(9) , 1499-505, (2014) Recent studies have highlighted the high sensitivity of PET imaging with (68)Ga-labeled octreotide derivatives for the detection and staging of neuroendocrine tumors. A somatostatin receptor ligand th... |
Fmoc-(D)-Phe-NH2 |
(R)-Fmoc-phenylalanine |
fmoc-d-phe |
N-Fmoc-D-phenylalanine |
D-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]- |
Fmoc-D-Phe-OH |
Fmoc-D-phenylalanine-OH |
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine |
MFCD00062955 |
Fmoc-D-phenylalanine |
Fmoc-phenylalanine |