CAS 62129-44-6
:N-tert-Butoxycarbonyl-4-iodo-L-phenylalanine
Description:
N-tert-Butoxycarbonyl-4-iodo-L-phenylalanine, commonly referred to as Boc-4-iodo-L-Phe, is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group and an iodine atom at the para position of the phenyl ring. This compound is typically used in peptide synthesis, particularly in the formation of peptides where selective protection of the amino group is required. The Boc group enhances the stability of the amino acid during synthetic procedures and can be removed under mild acidic conditions. The iodine substituent can facilitate further reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile building block in organic synthesis. The compound is generally solid at room temperature and is soluble in organic solvents, which aids in its handling and application in laboratory settings. Its molecular structure contributes to its reactivity and utility in various chemical transformations, particularly in the field of medicinal chemistry and peptide research.
Formula:C14H18INO4
InChI:InChI=1S/C14H18INO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
InChI key:InChIKey=JZLZDBGQWRBTHN-NSHDSACASA-N
SMILES:C([C@H](NC(OC(C)(C)C)=O)C(O)=O)C1=CC=C(I)C=C1
Synonyms:- (S)-2-(tert-Butoxycarbonylamino)-3-(4-iodophenyl)propanoic acid
- <span class="text-smallcaps">L</span>-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-iodo-
- Boc-L-4-Iodophenylalanine
- Boc-L-Phe(4-I)-OH
- Boc-Phe(4-I)-OH
- N-(tert-Butoxycarbonyl)-p-iodo-<span class="text-smallcaps">L</span>-phenylalanine
- N-BOC-4-Iodo-<span class="text-smallcaps">L</span>-phenylalanine
- N-[(1,1-Dimethylethoxy)carbonyl]-4-iodo-<span class="text-smallcaps">L</span>-phenylalanine
- N-tert-Butoxycarbonyl-4-iodo-<span class="text-smallcaps">L</span>-phenylalanine
- L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-iodo-
- N-BOC-4-Iodo-L-phenylalanine
- N-[(1,1-Dimethylethoxy)carbonyl]-4-iodo-L-phenylalanine
- N-(tert-Butoxycarbonyl)-p-iodo-L-phenylalanine
- See more synonyms
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Found 7 products.
N-Boc-4-iodo-L-phenylalanine, 98%
CAS:<p>N-Boc-4-iodo-L-phenylalanine is used as pharmaceutical intermediate. It is also used as a p-iodo phenyl alanine derivative with N-Boc protection. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer</p>Formula:C14H18INO4Purity:98%Molecular weight:391.21Boc-4-Iodo-L-Phenylalanine
CAS:Formula:C14H18INO4Purity:98%Color and Shape:SolidMolecular weight:391.2015Boc-Phe(4-I)-OH
CAS:Formula:C14H18INO4Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:391.214-Iodo-L-phenylalanine, N-BOC protected
CAS:4-Iodo-L-phenylalanine, N-BOC protectedFormula:C14H18INO4Purity:98%Color and Shape: white to off-white solidMolecular weight:391.20g/molBoc-Phe(4-I)-OH
CAS:Formula:C14H18INO4Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:391.21Boc-4-iodo-L-phenylalanine
CAS:<p>Boc-4-iodo-L-phenylalanine is a chemical compound belonging to the category of amino acid derivatives. It is widely used in research for various applications, including peptide synthesis and drug discovery.<br>The L-phenylalanine derivative, has a Boc protecting group (tert-butoxycarbonyl) on the amino group and an iodine atom at the 4-position of the phenyl ring. The Boc group protects the amino group from unwanted reactions during peptide synthesis, while the iodine atom serves as a useful group for further modifications.</p>Formula:C14H18IHO4Purity:Min. 95%Color and Shape:PowderMolecular weight:378.2 g/molBoc-4-Iodo-phenylalanine
CAS:<p>M03184 - Boc-4-Iodo-phenylalanine</p>Formula:C14H18INO4Purity:98%Color and Shape:Solid, PowderMolecular weight:391.205






