CAS 3303-84-2
:BOC-β-alanina
Descripción:
BOC-β-alanina, también conocido como tert-butoicocarbonilo-β-alanina, es un derivado de aminoácido caracterizado por la presencia de un grupo protector tert-butoicocarbonilo (BOC) unido al grupo amino de la β-alanina. Este compuesto se utiliza típicamente en la síntesis de péptidos y como un bloque de construcción en química orgánica debido a su capacidad para proteger la funcionalidad amina durante varias reacciones. BOC-β-alanina es un sólido blanco a blanco sucio que es soluble en disolventes orgánicos como el diclorometano y el dimetilformamida, pero menos soluble en agua. Su estructura molecular incluye un grupo ácido carboxílico, un grupo amino y un β-carbono, lo que contribuye a su clasificación como un β-aminoácido. El grupo BOC se puede eliminar en condiciones ácidas, permitiendo la regeneración del grupo amino libre para transformaciones químicas adicionales. BOC-β-alanina es valorado por su estabilidad y facilidad de manejo, lo que lo convierte en un reactivo útil en aplicaciones de química orgánica sintética y bioquímica.
Fórmula:C8H15NO4
InChI:InChI=1S/C8H15NO4/c1-8(2,3)13-7(12)9-5-4-6(10)11/h4-5H2,1-3H3,(H,9,12)(H,10,11)
Clave InChI:InChIKey=WCFJUSRQHZPVKY-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(NCCC(O)=O)=O
Sinónimos:- 3-(tert-Butoxycarbonylamino)propanoic acid
- 3-(tert-Butoxycarbonylamino)propionic acid
- 3-[(2-Methylpropan-2-yl)oxycarbonylamino]propanoic acid
- 3-[(Tert-Butoxycarbonyl)Amino]Propanoate
- 3-[N-(tert-Butoxycarbonyl)amino]propionic acid
- BOC-3-aminopropanoic acid
- BOC-beta-Alanine
- Boc-3-aminopropionic acid
- Boc-b-alanine
- Boc-beta-Ala
- Boc-beta-Ala-OH
- Boc-ß -Ala-OH
- Boc-β-Ala-OH
- Butoxycarbonylalanine
- N-(t-Butoxycarbonyl)-β-alanine
- N-(tert-Butoxycarbonyl)-3-aminopropionic acid
- N-(tert-Butyloxycarbonyl)-β-alanine
- N-Boc-3-aminopropanoic acid
- N-Boc-β-alanine
- N-T-boc-B-alanine crystalline
- N-[(1,1-Dimethylethoxy)carbonyl]-β-alanine
- N-[(t-Butyloxy)carbonyl]-β-alanine
- N-tert-Butoxycarbonyl-3-aminopropanoic acid
- N-tert-Butoxycarbonyl-β-alanine
- β-Alanine, N-[(1,1-dimethylethoxy)carbonyl]-
- β-Alanine, N-carboxy-, N-tert-butyl ester
- N-(tert-Butoxycarbonyl)-beta-alanine
- Ver más sinónimos
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Encontrado 9 productos.
3-tert-Butoxycarbonylaminopropionic acid
CAS:Fórmula:C8H15NO4Pureza:97%Forma y color:Solid, Crystalline Powder or PowderPeso molecular:189.211N-Boc-β-alanine, 99%
CAS:<p>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 Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Fórmula:C8H15NO4Pureza:99%Forma y color:White, Crystals or powder or crystalline powderPeso molecular:189.21Ref: IN-DA003STN
5g20,00€10g21,00€25g20,00€50g25,00€5kg537,00€100g31,00€10kgA consultar250g60,00€25kgA consultar500g83,00€50kgA consultarN-(tert-Butoxycarbonyl)-β-alanine
CAS:Fórmula:C8H15NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:189.21β-Alanine, N-BOC protected
CAS:<p>β-Alanine, N-BOC protected</p>Fórmula:C8H15NO4Pureza:98%Forma y color: white to light yellow solidPeso molecular:189.21g/molBoc-ß-Ala-OH
CAS:<p>Boc-ß-Ala-OH is an amino acid that inhibits the activity of gamma-aminobutyric acid (GABA) receptors. It has been shown to bind to the GABA receptor and block its activation by GABA. Boc-ß-Ala-OH is used as a building block for peptide synthesis, where it can be coupled with other amino acids to form a desired peptide sequence. This amino acid also possesses intramolecular hydrogen bonding interactions, which have been found to contribute to its inhibitory properties. Boc-ß-Ala-OH has a phase transition temperature of 104°C and is soluble in water below this point.</p>Fórmula:C8H15NOPureza:Min. 95%Peso molecular:189.21 g/molBOC-β-alanine
CAS:<p>BOC-β-alanine is a trifluoroacetic acid derivative that is activated with carbodiimides to form the ester hydrochloride. It has been shown to have anticancer activity in vitro and in vivo. BOC-β-alanine inhibits the synthesis of polypeptides by binding to the carboxyl group on the amino acid, thereby preventing protein formation. This compound also has an inhibitory effect on cell proliferation of 3T3-L1 preadipocytes in culture, which may be due to its ability to deplete fibrinogen from cells and inhibit activation of adenyl cyclase.</p>Fórmula:C8H15NO4Forma y color:White PowderPeso molecular:189.21 g/molBoc-β-Ala-OH
CAS:Producto controlado<p>Applications Boc-β-Ala-OH is a reagent used in the synthesis of quinazolines as platelet aggregation inhibitors and ligands of integrin.<br>References Krysko, A. et al.: Bioorg. Med. Chem. Lett., 26, 1839 (2016);<br></p>Fórmula:C8H15NO4Forma y color:NeatPeso molecular:189.21







