Specification
Synonyms
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-iodo-L-phenylalanine, Fmoc-4-Iodo-L-Phenylalanine, (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-iodophenyl)propanoic acid
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-iodophenyl)propanoic acid
Canonical SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC=C(C=C4)I)C(=O)O
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
Boiling Point
658.8±55.0 ℃at 760 mmHg
Melting Point
213-217 ℃(lit.)
Application
Fmoc-4-iodo-L-phenylalanine has numerous applications in scientific experiments, including peptide synthesis, drug discovery, and radioligand imaging studies. The compound is used as a building block for bioactive peptides and can be incorporated into pharmaceutical drugs to enhance their activity. Fmoc-4-iodo-L-phenylalanine can also be used as a radioligand for imaging studies in PET.
Type
Unusual Amino Acids, Analogs of Phenylalanine and Tyrosine
Vapor Pressure
0.0±2.1 mmHg at 25℃