CAS 2133-40-6
:L-Prolina, éster metílico, clorhidrato (1:1)
Descripción:
L-Prolina, éster metílico, clorhidrato (1:1) es un compuesto químico que sirve como un derivado del aminoácido prolina. Se caracteriza por la presencia de un grupo éster metílico, que mejora su solubilidad en disolventes orgánicos y puede influir en su actividad biológica. La forma de clorhidrato indica que el compuesto es una sal, lo que típicamente mejora la estabilidad y solubilidad en soluciones acuosas. Este compuesto se utiliza a menudo en la síntesis de péptidos y como un intermedio en la síntesis orgánica debido a su capacidad para participar en varias reacciones químicas. La L-Prolina en sí misma es un aminoácido no esencial que juega un papel crucial en la síntesis de proteínas y está involucrada en varios procesos metabólicos. La modificación del éster metílico puede afectar la reactividad del compuesto y su interacción con sistemas biológicos. Como con muchas sustancias químicas, el manejo debe hacerse con cuidado, adhiriéndose a los protocolos de seguridad para evitar la exposición. En general, la L-Prolina, éster metílico, clorhidrato es un compuesto valioso tanto en aplicaciones de investigación como industriales.
Fórmula:C6H11NO2·ClH
InChI:InChI=1S/C6H11NO2.ClH/c1-9-6(8)5-3-2-4-7-5;/h5,7H,2-4H2,1H3;1H/t5-;/m0./s1
Clave InChI:InChIKey=HQEIPVHJHZTMDP-JEDNCBNOSA-N
SMILES:C(OC)(=O)[C@@H]1CCCN1.Cl
Sinónimos:- (2S)-(Methoxycarbonyl)pyrrolidine hydrochloride
- (2S)-2-(methoxycarbonyl)pyrrolidinium
- (S)-Methyl pyrrolidine-2-carboxylate hydrochloride
- (S)-Proline methyl ester hydrochloride
- (S)-Pyrrolidine-2-carboxylic acid methyl ester hydrochloride
- <span class="text-smallcaps">L</span>-Pro-OMe hydrochloride
- <span class="text-smallcaps">L</span>-Proline methyl ester monohydrochloride
- <span class="text-smallcaps">L</span>-Proline, methyl ester, hydrochloride
- <span class="text-smallcaps">L</span>-Proline, methyl ester, hydrochloride (1:1)
- H-Pro-OMe.HCl
- H-Pro-OMe・HCl
- Methyl <span class="text-smallcaps">L</span>-prolinate hydrochloride
- Methyl Prolinate
- Methyl Prolinate Hydrochloride (1:1)
- Methyl prolinate hydrochloride
- Methyl proline hydrochloride
- Proline, methyl ester, hydrochloride, <span class="text-smallcaps">L</span>-
- methyl L-prolinate
- methyl L-prolinate hydrochloride
- L-Proline, methyl ester, hydrochloride
- Proline, methyl ester, hydrochloride, L-
- Ver más sinónimos
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Encontrado 11 productos.
L-Proline Methyl Ester Hydrochloride
CAS:Fórmula:C6H11NO2·HClPureza:>98.0%(T)Forma y color:White to Almost white powder to crystalPeso molecular:165.62L-Proline methyl ester hydrochloride, 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:C6H12NO2Pureza:98+%Forma y color:White, Crystals or powder or crystalline powder or lumpsPeso molecular:130.17H-Pro-OMe · HCl
CAS:<p>Bachem ID: 4000661.</p>Fórmula:C6H11NO2·HClPureza:> 99%Forma y color:WhitePeso molecular:165.62L-Proline methyl ester, HCl
CAS:Fórmula:C6H12ClNO2Pureza:97%Forma y color:SolidPeso molecular:165.6180Methyl (2S)-pyrrolidine-2-carboxylate hydrochloride
CAS:<p>Methyl (2S)-pyrrolidine-2-carboxylate hydrochloride</p>Fórmula:C6H11NO2·ClHPureza:98%Forma y color: white solidPeso molecular:165.62g/molL-Proline methyl ester hydrochloride
CAS:Fórmula:C6H11NO2HClPureza:≥ 98.0%Forma y color:White powderPeso molecular:165.62L-Proline Methyl Ester Hydrochloride
CAS:<p>Stability Hygroscopic<br>Applications L-Proline Methyl Ester Hydrochloride (cas# 2133-40-6) is a compound useful in organic synthesis.<br></p>Fórmula:C6H11NO2·ClHForma y color:White To Off-WhitePeso molecular:165.618L-Proline methyl ester hydrochloride
CAS:<p>L-Proline methyl ester hydrochloride is an organic compound that is classified as a trifluoroacetic acid ester. It has significant antiproliferative activity and induces apoptotic cell death in colorectal carcinoma cells. L-Proline methyl ester hydrochloride also inhibits the proliferation of lymphocytes by inhibiting protein synthesis, which may be due to its conformational properties. L-Proline methyl ester hydrochloride is synthesized by reacting L-proline with trifluoroacetic acid and subsequently hydrolyzing the resulting ester with hydrochloric acid. The synthesis can be carried out in two steps: first, a chloride ion is added to the protonated form of the amine; second, the protonated form of the amine reacts with hydrophobic compounds such as dodecyl amines or ethyl acetate to form an alkyl group. This reaction can also be carried out using</p>Fórmula:C6H12ClNO2Forma y color:White PowderPeso molecular:165.62 g/molH-Pro-OMe.HCl
CAS:<p>M02956 - H-Pro-OMe.HCl</p>Fórmula:C6H12ClNO2Pureza:95%Forma y color:SolidPeso molecular:165.62L-Proline-2,5,5-d3 Methyl Ester Hydrochloride
CAS:Producto controlado<p>Applications L-Proline-2,5,5-d3 Methyl Ester Hydrochloride is an intermediate in the synthesis of L-Prolinamide-2,5,5-d3 (P755976), a proline based organocatalyst.<br>References Alberg, D., et al.: Bioorg. Med. Chem. Lett., 19, 3888 (2009), Huang, X., et al.: J. Phys. Chem., 114, 1068 (2010),<br></p>Fórmula:C6H8D3NO2•HClForma y color:NeatPeso molecular:168.64









