CAS 2026-48-4: 1-Butanol, 2-amino-3-metil-, (2S)-
Descripción:
1-Butanol, 2-amino-3-metil-, (2S)-, también conocido como (S)-2-amino-3-metil-1-butanol, es un compuesto orgánico caracterizado por su estructura de aminoalcohol. Presenta una estructura de butanol con un grupo amino (-NH2) y un grupo metilo (-CH3) unidos al segundo y tercer átomo de carbono, respectivamente. Este compuesto es una molécula quiral, con la designación (2S) que indica su estereoequilibrio específico. Típicamente es un líquido incoloro a amarillo pálido con un olor característico y es soluble en agua debido a la presencia del grupo hidroxilo (-OH). La presencia de ambos grupos funcionales, amino e hidroxilo, le permite participar en enlaces de hidrógeno, influyendo en sus propiedades físicas y reactividad. 1-Butanol, 2-amino-3-metil-, (2S)- se utiliza a menudo en diversas síntesis químicas y puede servir como un intermedio en la producción de productos farmacéuticos o agroquímicos. Su actividad biológica y posibles aplicaciones en química medicinal son áreas de investigación en curso.
Fórmula:C5H13NO
InChI:InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1
Clave InChI:InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
SMILES:[C@H](C(C)C)(CO)N
Sinónimos:- (+)-(S)-Valinol
- (+)-2-Amino-3-methyl-1-butanol
- (+)-Valinol
- (2S)-1-Hydroxy-3-methylbutan-2-amine
- (2S)-2-Amino-3-methyl-1-butanol
- (2S)-Valinol
- (S)-(+)-2-Amino-3-methyl-1-butanol
- (S)-2-Amino-3-methylbutanol
- 1-Butanol, 2-amino-3-methyl-, (S)-
- 1-Butanol, 2-amino-3-methyl-, <span class="text-smallcaps">L</span>-
- 1-Butanol, 2-amino-3-methyl-, L-
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Encontrado 11 productos.
(S)-(+)-2-Amino-3-methyl-1-butanol, 96%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Fórmula:C5H13NOPureza:96%Forma y color:Liquid after melting or solid, Clear colorless to white to light yellowPeso molecular:103.17L-Valinol
CAS:M03447 - L-ValinolFórmula:C5H13NOPureza:95%Forma y color:LiquidPeso molecular:103.16500091552734L-Valinol
CAS:Producto controladoApplications L-Valinol is used as a reagent in the synthesis of simple 1,3-thiazolidine-2-thione derivatives which can exhibit fungicidal activity. L-Valinol is also used as a reagent in the synthesis of small-molecule inhibitors of MDM2-p53 protein-protein interaction (MDM2 inhibitors) in clinical trials for the treatment of cancer. References Chen, N., et al.: Phosphorus Sulfur, 190, 112 (2015); Zhao, Y., et al.: J. Med. Chem., 58, 1038 (2015)Fórmula:C5H13NOForma y color:WhitePeso molecular:103.163L-(+)-Valinol, 97%
CAS:L-(+)-Valinol reacts with aldehydes and nitriles to form imines and oxazolines, respectively, for asymmetric synthesis. It is also used for preparation of 4-isopropyloxazolidinones, employed in stereocontrolled aldol and alkylation reactions, synthesis of chiral 2-thiazolidinethiones for aldol reactions, asymmetric alkylation of condensation product with keto acids, asymmetric reactions of its amidines and imines and oxidation of N-protected derivative to the aldehyde. 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 Scientific Chemicals.Fórmula:C5H13NOPureza:97%Forma y color:Colourless/white to yellow, liquid/low melting solidPeso molecular:103.17L-Valinol
CAS:Fórmula:C5H13NOPureza:>97.0%(GC)(T)Forma y color:White or Colorless to Light orange to Yellow powder to lump to clear liquidPeso molecular:103.17(S)-(+)-2-Amino-3-methyl-1-butanol
CAS:(S)-(+)-2-Amino-3-methyl-1-butanolFórmula:C5H13NOPureza:97%Forma y color: colourless to light yellow crystalline solidPeso molecular:103.16g/molL-Valinol
CAS:L-Valinol is a model system that is used to study the reaction of aziridines with oxygen nucleophiles. It has been shown that this reaction proceeds through the formation of an intermediate, hydrogen tartrate, followed by a second step with nitrogen atoms as the nucleophile and alcohol residue as the substrate. The use of L-valinol in asymmetric synthesis was also demonstrated. In this process, amides were obtained with high enantioselectivity by reacting L-valinol with amines in acidic conditions. This synthetic pathway was found to be synergic with other reactions, such as nitroolefination and benzoylation.Fórmula:C5H13NOPureza:Min. 95%Forma y color:Solidified MassPeso molecular:103.16 g/molL-Valinol
CAS:Fórmula:C5H13NOPureza:≥ 97.0%Forma y color:Colourless to white or pale yellow solid, crystals or liquidPeso molecular:103.17
