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Merck
CN

47378

Fmoc-D-Phe-OH

≥98.0%

Synonym(s):

Fmoc-D-phenylalanine

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About This Item

Empirical Formula (Hill Notation):
C24H21NO4
CAS Number:
86123-10-6
Molecular Weight:
387.43
Beilstein:
4767931
MDL number:
MFCD00062955
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57650934
NACRES:
NA.26

Key Documents

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Assay

≥98.0%

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

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-/m1/s1

InChI key

SJVFAHZPLIXNDH-JOCHJYFZSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4414
BCCD6373
BCBX1620
BCBD1834V
BCBR7430V

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Zhibo Liu et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(9), 1499-1505 (2014-06-28)
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Oliver John V Belleza et al.
MedChemComm, 9(10), 1673-1678 (2018-11-16)
Nobilamide B, a TRPV1 antagonist, and a series of Ala-substituted analogues were synthesized and their neuroactivity was assessed in a primary culture of dorsal root ganglion (DRG) neurons. Analogues 4, 6, and 7 showed comparable activity, affecting capsaicin response in
Charles A Galea et al.
Biochemistry, 56(4), 657-668 (2017-01-11)
Polymyxins remain one of the few antibiotics available for treating antibiotic resistant bacteria. Here we describe polymyxin B thioesterase which performs the final step in polymyxin B biosynthesis. Isolated thioesterase catalyzed cyclization of an N-acetylcystamine polymyxin B analogue to form
Jingfang Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(54), 13510-13517 (2017-07-12)
A series of cationic peptides with alternating hydrophilic and hydrophobic residues were elaborately designed and synthesized. These kinds of short peptides with protonated lysine groups can interact with anionic polyoxometalate nanoclusters through multivalent ionic bonds and hydrogen bonds, resulting in
Kazuma Ogawa et al.
Chemical & pharmaceutical bulletin, 66(6), 651-659 (2018-06-05)
Radiolabeled cyclic peptides containing the (Arg-Gly-Asp) RGD sequence for use in positron emission tomography (PET) imaging, single-photon emission computed tomography (SPECT) imaging, and targeted radionuclide therapy of cancer have been reported. In this study, RGD was used as a model
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