CAS 13734-41-3
:Boc-L-valine
Description:
Boc-L-valine, or tert-butoxycarbonyl-L-valine, is a protected form of the amino acid valine, commonly used in peptide synthesis and organic chemistry. It features a tert-butoxycarbonyl (Boc) group, which serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amino group. The compound is typically a white to off-white crystalline solid and is soluble in organic solvents such as dichloromethane and dimethylformamide, but less soluble in water. Boc-L-valine is characterized by its chirality, as it contains a chiral center at the alpha carbon, making it an L-enantiomer. This property is crucial in biological systems and pharmaceutical applications, where the specific stereochemistry can significantly influence activity and efficacy. The compound is stable under standard laboratory conditions but can be hydrolyzed under acidic or basic conditions, releasing the free amino acid valine. Its applications extend to the synthesis of peptides, where the Boc group can be removed under mild acidic conditions, facilitating further reactions.
Formula:C10H19NO4
InChI:InChI=1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1
InChI key:InChIKey=SZXBQTSZISFIAO-ZETCQYMHSA-N
SMILES:[C@H](NC(OC(C)(C)C)=O)(C(C)C)C(O)=O
Synonyms:- (2S)-2-(tert-Butoxycarbonylamino)-3-methylbutanoic acid
- (2S)-2-[(tert-butoxycarbonyl)amino]-3-methylbutanoate
- (2S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-methylbutanoic acid
- (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-methylbutanoic acid
- (2S)-3-Methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
- (S)-2-(Boc-Amino)-3-Methylbutyric Acid
- (S)-2-(tert-Butoxycarbonylamino)-3-methylbutanoic acid
- (S)-Boc-Valine
- (S)-N-tert-Butoxycarbonylvaline
- <span class="text-smallcaps">L</span>-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
- BOC-valine
- Boc-<span class="text-smallcaps">L</span>-Val
- Boc-<span class="text-smallcaps">L</span>-valine
- Boc-L-Valine
- Boc-Val-OH
- Boc-l-Val-OH
- L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
- N-(tert-butoxycarbonyl)-D-valine
- N-(tert-butoxycarbonyl)-L-valine
- N-(tert-butoxycarbonyl)valine
- N-BOC-<span class="text-smallcaps">L</span>-valine
- N-BOC-valine
- N-Boc-L-Valine
- N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-valine
- N-[(1,1-Dimethylethoxy)carbonyl]-L-valine
- N-[(terc-butoxi)carbonil]-L-valina
- N-[(tert-Butoxy)carbonyl]-L-valin
- N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valine
- N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valine vinyl ester
- N-tert-Butoxycarbonylvaline
- N-tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-valine
- N-tert-Butyloxycarbonyl-L-valine
- N-tert-Butyloxycarbonylvaline
- N-α-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valine
- N-α-tert-Butoxycarbonyl-L-valine
- Nsc 197197
- Valine, N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-
- Valine, N-carboxy-, N-tert-butyl ester, L-
- t-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valine
- t-Butoxycarbonyl-L-valine
- tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-valine
- See more synonyms
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Found 13 products.
N-(tert-Butoxycarbonyl)-L-valine
CAS:Formula:C10H19NO4Purity:>99.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:217.27Boc-Val-OH
CAS:<p>M03340 - Boc-Val-OH</p>Formula:C10H19NO4Purity:98%Color and Shape:Solid, Powder or Crystalline Powder or SolidMolecular weight:217.265N-Boc-L-valine, 98+%
CAS:<p>N-Boc-L-valine is used in the multi-peptide synthesis and serves as the amino acid protection monomer. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aes</p>Formula:C10H19NO4Purity:98+%Color and Shape:White, PowderMolecular weight:217.27Boc-Val-OH
CAS:<p>Bachem ID: 4000426.</p>Formula:C10H19NO4Purity:100.0%Color and Shape:WhiteMolecular weight:217.27N-t-butyloxycarbonyl-N-methyl-L-valine
CAS:Formula:C10H19NO4Purity:97%Color and Shape:SolidMolecular weight:217.2622N-(tert-Butoxycarbonyl)-L-valine
CAS:N-(tert-Butoxycarbonyl)-L-valineFormula:C10H19NO4Purity:99%Color and Shape: white to off-white solidMolecular weight:217.26g/molBOC-L-Valine extrapure, 99%
CAS:Formula:C10H19NO4Purity:min. 99%Color and Shape:White to off-white, Crystalline powderMolecular weight:217.30Boc-L-Valine
CAS:Controlled Product<p>Applications Boc-L-Valine is used in amino acid conjugates as proteasome inhibitors.<br>References Wan, S. et al.: Int. J. Mol. Med., 26, 447 (2010);<br></p>Formula:C10H19NO4Color and Shape:NeatMolecular weight:217.26Boc-Val-OH
CAS:<p>Boc-Val-OH is a natural compound that belongs to the class of ferrocene fatty acid. It has been shown to have antimicrobial properties in cell culture and pharmacokinetic properties in rats. Boc-Val-OH is able to inhibit the activity of serine proteases, which are enzymes that break down proteins and amino acids within cells, as well as cyclopropavir, a virus inhibitor. This compound also has potent inhibitory activity against various microbial strains, including methicillin-resistant Staphylococcus aureus (MRSA) and Helicobacter pylori. Boc-Val-OH has been shown to have hepatoprotective effects in rats with liver damage.</p>Formula:C10H19NO4Purity:Min. 95%Molecular weight:217.26 g/molBoc-L-valine
CAS:<p>Boc-L-Valine is a model system for the synthesis of peptides. This compound is synthesized in a liquid phase and then purified by column chromatography. It has an antimicrobial activity against Gram-positive bacteria such as Staphylococcus aureus and Escherichia coli, but not against Gram-negative bacteria such as Proteus vulgaris or Pseudomonas aeruginosa. Boc-L-Valine is also used to study the binding of inhibitors and ferrocenes.</p>Formula:C10H19NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:217.3 g/mol











