CAS 27317-69-7
:N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl-L-alanine
Description:
N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl-L-alanine, with the CAS number 27317-69-7, is a synthetic compound that belongs to the class of amino acid derivatives. This substance features a dipeptide structure, consisting of two L-alanine residues linked by a peptide bond, with a protective group (1,1-dimethylethoxycarbonyl) attached to one of the amino groups. The presence of the bulky dimethylethoxycarbonyl group enhances the stability and solubility of the compound, making it useful in peptide synthesis and pharmaceutical applications. The compound is typically white to off-white in appearance and is soluble in polar organic solvents. Its molecular structure allows for potential applications in drug development, particularly in the design of prodrugs or in the synthesis of more complex peptides. As with many amino acid derivatives, it may exhibit biological activity, although specific pharmacological properties would require further investigation. Proper handling and storage conditions should be observed due to its chemical nature.
Formula:C11H20N2O5
InChI:InChI=1S/C11H20N2O5/c1-6(8(14)12-7(2)9(15)16)13-10(17)18-11(3,4)5/h6-7H,1-5H3,(H,12,14)(H,13,17)(H,15,16)/t6-,7-/m0/s1
InChI key:InChIKey=BZNDDHWTEVCBAD-BQBZGAKWSA-N
SMILES:N([C@H](C(N[C@H](C(O)=O)C)=O)C)C(OC(C)(C)C)=O
Synonyms:- <span class="text-smallcaps">L</smallcap>-Alanine, N-[(1,1-dimethylethoxy)carbonyl]-<smallcap>L</span>-alanyl-
- <span class="text-smallcaps">L</smallcap>-Alanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-<smallcap>L</span>-alanyl]-
- Alanine, N-(N-carboxy-<span class="text-smallcaps">L</smallcap>-alanyl)-, N-tert-butyl ester, <smallcap>L</span>-
- N-(tert-butoxycarbonyl)alanylalanine
- N-Boc-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine
- N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine
- N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine
- N-tert-Butoxycarbonylalanylalanine
- NSC 334362
- tert-Butoxycarbonyl-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine
- N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl-L-alanine
- L-Alanine, N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-
- Alanine, N-(N-carboxy-L-alanyl)-, N-tert-butyl ester, L-
- L-Alanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-
- See more synonyms
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Found 6 products.
Boc-Ala-Ala-OH
CAS:<p>Bachem ID: 4001154.</p>Formula:C11H20N2O5Purity:> 99%Color and Shape:White PowderMolecular weight:260.29Boc-Ala-Ala-OH
CAS:<p>Boc-Ala-Ala-OH is an amide of the amino acid alanine with a hydroxyl group. This compound has been synthesized as a stable complex with enzymes and is used in enzymatic methods to study peptidase activity. Boc-Ala-Ala-OH inhibits the enzyme by forming a covalent bond with the hydroxyl group on the enzyme's active site, which prevents it from interacting with its substrate, leading to inhibition of enzymatic activity. Boc-Ala-Ala-OH binds to mammalian cells and lysosomal systems and can be used as a probe for studying proteolytic enzyme activity in cells. Spectrometric data shows that Boc-Ala-Ala-OH is an easily activated molecule and may be useful in synthetic studies.</p>Formula:C11H20N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:260.29 g/molN-Boc-L-alanyl-L-alanine
CAS:Controlled Product<p>Applications N-Phthalyl-alanine is used in the preparation of endothiopeptide inhibitors of HIV-1 Protease.<br>References Yao, S., et al.: J. Bioorg. Med. Chem. Lett., 8, 699, 1998<br></p>Formula:C11H20N2O5Color and Shape:NeatMolecular weight:260.29





