CAS 37784-17-1
:N-Boc-D-prolina
Descripción:
N-Boc-D-prolina, con el número CAS 37784-17-1, es un derivado del aminoácido prolina, caracterizado por la presencia de un grupo protector tert-butyloxycarbonyl (Boc) en el átomo de nitrógeno. Esta modificación mejora su estabilidad y solubilidad, lo que lo convierte en un intermediario valioso en la síntesis de péptidos y la química orgánica. N-Boc-D-prolina es típicamente un sólido cristalino blanco a blanco sucio, y es soluble en disolventes orgánicos comunes como el diclorometano y el dimetilformamida, pero menos soluble en agua. El grupo Boc actúa como un moiety protector que puede ser eliminado en condiciones ácidas, permitiendo la deprotección selectiva del grupo amino cuando sea necesario. Este compuesto se utiliza a menudo en la síntesis de péptidos y otras moléculas bioactivas, gracias a su capacidad para facilitar la formación de enlaces peptídicos mientras mantiene la quiralidad del residuo D-prolina. Sus características estructurales y reactividad lo convierten en un bloque de construcción importante en la química medicinal y el desarrollo de fármacos.
Fórmula:C10H16NO4
InChI:InChI=1/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/p-1/t7-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC[C@@H]1C(=O)[O-]
Sinónimos:- (2R)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylate
- 1-Boc-D-proline
- Boc-D-Pro-OH
- Boc-D-proline
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 12 productos.
N-(tert-Butoxycarbonyl)-D-proline
CAS:Fórmula:C10H17NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:215.25N-Boc-D-proline, 98+%
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:C10H17NO4Pureza:98+%Forma y color:White, Crystals or powder or crystalline powderPeso molecular:215.25Boc-D-Pro-OH
CAS:<p>Bachem ID: 4000664.</p>Fórmula:C10H17NO4Pureza:> 99.5%Forma y color:WhitePeso molecular:215.25Ref: IN-DA0035CW
5g20,00€10g25,00€1kg190,00€25g29,00€50g35,00€5kgA consultar100g56,00€10kgA consultar500g135,00€N-Boc-D-proline
CAS:<p>N-Boc-D-proline</p>Pureza:98%Forma y color:White PowderPeso molecular:215.25g/molN-Boc-D-proline
CAS:Fórmula:C10H17NO4Pureza:≥ 98.0%Forma y color:White powder or crystalsPeso molecular:215.25Boc-D-Pro-OH
CAS:<p>M03316 - Boc-D-Pro-OH</p>Fórmula:C10H17NO4Pureza:97%Forma y color:Solid, Crystalline Powder or PowderPeso molecular:215.249tert-Butoxycarbonyl-D-proline
CAS:Producto controlado<p>Applications tert-Butoxycarbonyl-D-proline is Boc protected D-proline (P755990). It is used to prepare trichostatin A and trapoxin B analogs as histone deacetylase inhibitors. It is also used to prepare potent and selective nonpeptide inhibitors of caspases 3 and 7.<br>References Jung, M., et al.: Bioorg. Med. Chem. Lett., 7, 1655 (1997); Lee, D., et al.: J. Med. Chem,, 44, 2015 (2001)<br></p>Fórmula:C10H17NO4Forma y color:NeatPeso molecular:215.25N-Boc-D-proline
CAS:<p>N-Boc-D-proline is a lipase inhibitor that is used in the preparation of quinine, aldehyde, and carboxylate. N-Boc-D-proline has been shown to inhibit the activity of the sodium channels, which may be due to its ability to bind to the termini of these channels. The inhibition of sodium channels can lead to a decrease in nerve excitability and seizures. N-Boc-D-proline was synthesized by an organocatalytic method using sodium bicarbonate as the catalyst. It was found that this compound was stereoselective with respect to its activity on different enantiomers of chiral substrates. Preparative methods for N-Boc-D-proline include column chromatography or crystallization with diethyl ether or ethyl acetate. The isolated yield is about 99%.</p>Fórmula:C10H17NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:215.25 g/molBoc-D-Pro-OH
CAS:<p>Boc-D-Pro-OH is a model compound for the synthesis of peptides. Boc-D-Pro-OH has been used in many surface-enhanced Raman spectroscopy studies to investigate the stereochemistry of glycosidic bonds. It has also been used in pharmacokinetic studies to investigate the drug's absorption, distribution, metabolism, and excretion (ADME) properties. The solute is soluble in water due to its hydrophilic nature. Boc-D-Pro-OH is an enantiomer of Boc-L-Pro-OH and a functional group that contains a trifluoromethyl group. This chemical can be used in Tools for Peptide Synthesis with other compounds to form peptides with specific amino acid sequences.</p>Fórmula:C10H17NO4Pureza:Min. 95%Peso molecular:215.25 g/molBOC-D-Proline extrapure, 99%
CAS:Fórmula:C10H17NO4Pureza:min. 99%Forma y color:White, Crystalline compoundPeso molecular:215.30










