Fmoc-D-Phe-OH

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Names

[ CAS No. ]:
86123-10-6

[ Name ]:
Fmoc-D-Phe-OH

[Synonym ]:
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

Chemical & Physical Properties

[ 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

MSDS

Click to get detail MSDS

Safety Information

[ 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

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • (R)-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl) 2-(((9Hfluoren-9-yl)methoxy)carbonyl)amino-3-phenylpropanoate
  • 9-Fluorenylmethyl chloroformate
  • D-phenylalanine
  • Fmoc-Osu

DownStream

  • 9-Methylene-9H-fluorene
  • D-phenylalanine
  • H-D-Phe-D-Phe-OH
  • Ac-D-Phe-OH
  • Fmoc-D-beta-homophenylalanine
  • Cyclo(-Arg-Gly-Asp-D-Phe-Lys) trifluoroacetate salt

Customs

[ 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%

Articles

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...


More Articles

Related Compounds

  • Fmoc-D-Phe-OH-d5
  • Fmoc-D-phe(3-OH)-OH
  • Fmoc-D-Phe(F5)-OH
  • Fmoc-D-phe(4-OCH3)-OH
  • fmoc-d-phe(2-i)-oh
  • Fmoc-D-Phe(4-NHBoc)-OH
  • CID 12198406
  • 5-Aminotetrahydro-2(1H)-pyrimidinon
  • Tert-butyl 3-iodopyrrole-1-carboxylate
  • N3-(3-Aminopropyl)-1,3-butanediamine
  • 4-[(Dimethylamino)phenylmethyl]-3-quinolinol
  • 5-amino-1-(4-methylphenyl)-2-oxo-3H-pyrrole-4-carbonitrile
  • (3R)-3-{[(benzyloxy)carbonyl]amino}-3-methylpentanoic acid
  • 9-Oxatricyclo[5.2.1.0,1,6]decan-5-one
  • 2-((4-(((Tert-butyldimethylsilyl)oxy)methyl)-3-methylpyridin-2-yl)amino)thiazole-5-carbonitrile
  • Pyrazol-3-ON,2(26dime-4pyrimd)15dime
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