Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

47378

Sigma-Aldrich

Fmoc-D-Phe-OH

≥98.0%

Synonym(s):

Fmoc-D-phenylalanine

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Quality Level

100

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

Looking for similar products? Visit Product Comparison Guide

related product

Product No.
Description
Pricing

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD6373
BCBX1620
BCBD1834V
BCBR7430V
BCBL3210V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Zhibo Liu et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(9), 1499-1505 (2014-06-28)
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 that is easily radiolabeled with (18)F-fluoride could improve the availability of PET imaging of
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
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
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service