CAS 13734-34-4
:N-Boc-L-phénylalanine
Description :
N-Boc-L-phénylalanine est un dérivé de l'acide aminé phénylalanine, caractérisé par la présence d'un groupe protecteur tert-butyloxycarbonyle (Boc) sur le groupe amino. Cette modification améliore sa stabilité et sa solubilité, la rendant utile dans la synthèse peptidique et d'autres réactions organiques. Le composé est typiquement un solide cristallin blanc à blanc cassé, et il est soluble dans des solvants organiques tels que le dichlorométhane et le diméthylsulfoxyde, mais moins soluble dans l'eau. N-Boc-L-phénylalanine est souvent utilisée dans la synthèse de peptides en raison de sa capacité à protéger le groupe amino lors des réactions de couplage, permettant des modifications sélectives. Sa structure comprend une chaîne latérale phénylique, qui contribue à ses caractéristiques hydrophobes, influençant ses interactions dans les systèmes biologiques. Le composé est également utilisé dans la recherche et le développement pharmaceutique, en particulier dans la conception de molécules biologiquement actives. Comme pour de nombreuses substances chimiques, une manipulation appropriée et des précautions de sécurité sont essentielles en raison des dangers potentiels associés à son utilisation.
Formule :C14H19NO4
InChI :InChI=1/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/p-1/t11-/m0/s1
Code InChI :InChIKey=ZYJPUMXJBDHSIF-NSHDSACASA-N
SMILES :[C@@H](CC1=CC=CC=C1)(NC(OC(C)(C)C)=O)C(O)=O
Synonymes :- (2S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropionic acid
- (2S)-2-(tert-Butoxycarbonylamino)-3-phenyl-propanoic acid
- (2S)-2-(tert-Butoxycarbonylamino)-3-phenylpropanoic acid
- (2S)-2-[(2-Methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid
- (2S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropanoate
- (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-phenylpropanoic acid
- (S)-2-(tert-Butoxycarbonylamino)-3-phenylpropanoic acid
- (S)-2-[(tert-Butoxycarbonyl)amino]-3-phenylpropionic acid
- (S)-N-(tert-Butoxycarbonyl)phenylalanine
- (S)-N-Boc-phenylalanine
- (tert-Butoxycarbonyl)phenylalanine
- <span class="text-smallcaps">L</span>-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
- Alanine, N-carboxy-3-phenyl-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-
- Alanine, N-carboxy-3-phenyl-, N-tert-butyl ester, L-
- BOC-<span class="text-smallcaps">L</span>-Phenylalanine
- BOC-L-Phe-OH
- Boc-<span class="text-smallcaps">L</span>-Phe-OH
- Boc-L-phenylalanine
- Boc-Phe-OH
- L-Phenyl-1-13C-alanine, N-t-BOC Derivative
- L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
- N-(Tert-Butoxycarbonyl)-L-Phenylalanine
- N-(terc-butoxicarbonil)-L-fenilalanina
- N-(tert-Butoxycarbonyl)-(S)-phenylalanine
- N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-phenylalanine
- N-(tert-Butoxycarbonyl)-L-phenylalanin
- N-(tert-Butyloxycarbonyl)-<span class="text-smallcaps">L</span>-phenylalanine
- N-(tert-Butyloxycarbonyl)-L-phenylalanine
- N-(tert-Butyloxycarbonyl)phenylalanine
- N-(tert-butoxycarbonyl)-D-phenylalanine
- N-(tert-butoxycarbonyl)phenylalanine
- N-Alpha-T-Butoxycarbonyl-L-Phenylalanine
- N-Alpha-Tert-Butyloxycarbonyl-L-Phenylalanine
- N-BOC-(S)-phenylalanine
- N-BOC-<span class="text-smallcaps">L</span>-phenylalanine
- N-BOC-phenylalanine
- N-Boc-L-Phenylalanine
- N-T-Boc-L-Phenylalanine
- N-T-Butoxycarbonyl-L-Phenylalanine
- N-Tert-Butyloxycarbonyl-Dl-Phenylalanine
- N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-phenylalanine
- N-[(1,1-Dimethylethoxy)carbonyl]-L-phenylalanine
- N-[(1,1-Dimethylethoxy)carbonyl]-N-L-phenylalanine
- N-alpha-t-BOC-L-phenylalanine
- N-t-BOC-<span class="text-smallcaps">L</span>-phenylalanine
- Nsc 111172
- tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-phenylalanine
- tert-Butoxycarbonyl-L-phenylalanine
- BOC-L-PHENYLALANINE-OH
- 2-BOC-AMINO-3-PHENYL-PROPIONIC ACID
- RARECHEM AL BE 0755
- BOC-L-PHE
- BOC-PHE
- (S)-2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONIC ACID
- BOC-PHENYLALANINE
- Voir plus de synonymes
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11 produits concernés.
N-(tert-Butoxycarbonyl)-L-phenylalanine
CAS :Formule :C14H19NO4Degré de pureté :>99.0%(T)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :265.31Boc-Phe-OH
CAS :<p>M03310 - Boc-Phe-OH</p>Formule :C14H19NO4Degré de pureté :98%Couleur et forme :Solid, Crystalline PowderMasse moléculaire :265.309N-Boc-L-phenylalanine, 99%
CAS :<p>N-Boc-L-phenylalanine is a derivative of Phenylalanine used in enantioselective hydrolysis of amino acid esters. 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 origina</p>Formule :C14H19NO4Degré de pureté :99%Couleur et forme :White, Crystals or powder or crystalline powderMasse moléculaire :265.31Boc-Phe-OH
CAS :<p>Bachem ID: 4000663.</p>Formule :C14H19NO4Degré de pureté :> 99%Couleur et forme :White PowderMasse moléculaire :265.31N-(tert-Butoxycarbonyl)-L-phenylalanine
CAS :Formule :C14H19NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :265.3050Boc-L-phenylalanine
CAS :<p>Boc-L-phenylalanine</p>Formule :C14H19NO4Degré de pureté :98.5%Couleur et forme : white solidMasse moléculaire :265.30g/molBoc-Phe-OH
CAS :<p>Boc-Phe-OH is a group P2, amide compound. It has been shown to exhibit anti-cancer activity and has been used in the synthesis of peptides. Boc-Phe-OH is an inhibitor of aminopeptidases and has been shown to inhibit the growth of herpes simplex virus. As a result, it is a useful tool for studying the biological function of these enzymes.</p>Formule :C14H19NO4Degré de pureté :Min. 95%Masse moléculaire :265.3 g/molN-Boc-L-phenylalanine
CAS :<p>N-Boc-L-phenylalanine is a metabolic intermediate that belongs to the class of chemical compounds. It is an amino acid that has been shown to be useful in the treatment of metabolic disorders such as phenylketonuria and hyperphenylalaninemia. N-Boc-L-Phenylalanine is used as a fluorescent derivative and can be synthesized by reacting with trifluoroacetic acid (TFA) and hydrogen bromide. This active methylene group can bind to pyrazine-2-carboxylic acid, which has been shown to inhibit the growth of lymphocytic leukemia cells in culture experiments. N-Boc-L-Phenylalanine also has a hydroxy group on its side chain, which makes it soluble in water and amenable for chromatographic purification methods.</p>Formule :C14H19NO4Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :265.31 g/molBOC-L-Phenylalanine extrapure, 99%
CAS :Formule :C14H19NO4Degré de pureté :min. 99%Couleur et forme :White to off-white, Crystalline powderMasse moléculaire :265.30N-Boc-L-phenylalanine
CAS :Produit contrôlé<p>Applications Phenylalanine derivative used in enantioselective hydrolysis of amino acid esters. Acts as an inhibitor of gastric acid secretion.<br>References Tomisaka, K. et al.: Chem. Comm., 1, 133 (2001); Magours, R., et al.: Biochim. Biophys. Acta, Mol. Cell Res., 858, 158 (1985)<br></p>Formule :C14H19NO4Couleur et forme :NeatMasse moléculaire :265.3
