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Sigma-Aldrich

Fmoc-Phe-OH

98%, for peptide synthesis

Sinónimos:

N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine, Fmoc-L-phenylalanine

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About This Item

Fórmula empírica (notación de Hill):
C24H21NO4
Número de CAS:
35661-40-6
Peso molecular:
387.43
Beilstein/REAXYS Number:
3597808
EC Number:
252-661-1
MDL number:
MFCD00037128
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24860536
NACRES:
NA.26

product name

Fmoc-Phe-OH, 98%

assay

98%

optical activity

[α]20/D −37°, c = 1 in DMF

reaction suitability

reaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

mp

180-187 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc
amine
carboxylic acid

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](Cc1ccccc1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m0/s1

InChI key

SJVFAHZPLIXNDH-QFIPXVFZSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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European journal of medicinal chemistry, 44(5), 1933-1940 (2008-12-27)
Twenty-four new dipeptide analogs (1-24) of aurantiamide acetate were designed, synthesized, and assayed for effects on superoxide anion generation and elastase release by human neutrophils in response to fMLP/CB. Among them, seven N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides (6, 9, 12, 14, 17, 18
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