Boc-Ile-OH • 1/2 H2O

CAS : 13139-16-7

Ref. 3D-BLI-2065

Informations sur le produit

• Nom: Boc-Ile-OH • 1/2 H2O
• Synonymes: (2S,3R)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoate, (2S,3S)-2-(tert-Butoxycarbonylamino)-3-methylpentanoic acid, (2S,3S)-2-[(tert-Butoxycarbonyl)amino]-3-methylpentanoic acid, (2S,3S)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoate, <span class="text-smallcaps">L</span>-Isoleucine, N-[(1,1-dimethylethoxy)carbonyl]-, BOC-<span class="text-smallcaps">L</span>-isoleucine, BOC-isoleucine, Boc-Ile-OH, Boc-L-Ile-OH, Boc-L-isoleucine, Isoleucine, N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-, Isoleucine, N-carboxy-, N-tert-butyl ester, L-, L-Isoleucine, N-[(1,1-dimethylethoxy)carbonyl]-, N-(terc-butoxicarbonil)-L-isoleucina, N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-isoleucine, N-(tert-Butoxycarbonyl)-L-isoleucin, N-(tert-Butyloxycarbonyl)-<span class="text-smallcaps">L</span>-isoleucine, N-(tert-Butyloxycarbonyl)-L-isoleucine, N-(tert-butoxycarbonyl)-D-alloisoleucine, N-(tert-butoxycarbonyl)-D-isoleucine, N-(tert-butoxycarbonyl)-L-alloisoleucine, N-(tert-butoxycarbonyl)isoleucine, N-Boc-<span class="text-smallcaps">L</span>-isoleucine, N-Carboxyisoleucine N-tert-butyl ester, N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-isoleucine, N-[(1,1-Dimethylethoxy)carbonyl]-L-isoleucine, N-t-Boc-<span class="text-smallcaps">L</span>-isoleucine, N-t-Boc-L-isoleucine, N-tert-Butoxycarbonylisoleucine, Nsc 334311, Tert-Butyl Beta-Alaninate, tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-isoleucine, tert-Butoxycarbonyl-L-isoleucine, N-(tert-Butoxycarbonyl)-L-isoleucine

Description

Boc-Ile-OH • 1/2 H2O is a synthetic monomer that can be used in peptide synthesis. It is detectable under microscopy and chromatography, and is a component of the Tool for Peptide Synthesis. Boc-Ile-OH • 1/2 H2O has a nature that is synthetic and industrialized, an amino acid composition that is synthetic, and can be used as a monomer in polymerization reactions. This compound also shows enhancement of acidic radical chain reactions. The chromatographic method used to identify this compound utilizes TLC on alumina plates, which are then sprayed with ninhydrin reagent or phosphomolybdic acid reagent. The plate is heated until the solvent evaporates and the residue remains on the plate.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 240.3 g/mol
• Formule: C₁₁H₂₁NO₄H₂O
• Degré de pureté: Min. 95%