Skip to Content
Merck
All Photos(1)

Key Documents

47431

Sigma-Aldrich

Fmoc-Phe(4-I)-OH

≥97.0%

Synonym(s):

Fmoc-4-iodo-L-phenylalanine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C24H20INO4
CAS Number:
Molecular Weight:
513.32
Beilstein:
4592723
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

Assay

≥97.0%

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](Cc1ccc(I)cc1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C24H20INO4/c25-16-11-9-15(10-12-16)13-22(23(27)28)26-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1

InChI key

LXOXXTQKKRJNNB-QFIPXVFZSA-N

Other Notes

Synthesis of a phosphotyrosine mimetic; Building block employed for the synthesis of peptides carrying a radio-label

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

R.E. Shute et al.
Tetrahedron Letters, 28, 3419-3419 (1987)
M.N. Qabar et al.
Tetrahedron, 53, 11171-11171 (1997)
Xiaoyan Mu et al.
Physical chemistry chemical physics : PCCP, 19(25), 16923-16933 (2017-06-21)
Four isomers of the radical cation of tripeptide phenylalanylglycyltryptophan, in which the initial location of the radical center is well defined, have been isolated and their collision-induced dissociation (CID) spectra examined. These ions, the π-centered [FGW
Sandra Ortega Ugalde et al.
Biochemical pharmacology, 177, 113938-113938 (2020-04-01)
Tuberculosis (TB) is a globally significant infective disease that is caused by a single infectious agent, Mycobacterium tuberculosis (Mtb). Because of the rise in the number of multidrug-resistant (MDR) TB strains, identification of alternative drug targets for the development of
Anirban Banerjee et al.
eLife, 2, e00594-e00594 (2013-05-25)
Pore-blocking toxins inhibit voltage-dependent K(+) channels (Kv channels) by plugging the ion-conduction pathway. We have solved the crystal structure of paddle chimera, a Kv channel in complex with charybdotoxin (CTX), a pore-blocking toxin. The toxin binds to the extracellular pore

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