184837
2-Amino-3-methyl-1-butanol
97%
Sinónimos:
DL-Valinol
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About This Item
Fórmula lineal:
(CH3)2CHCH(NH2)CH2OH
Número de CAS:
Peso molecular:
103.16
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
Productos recomendados
Ensayo
97%
Formulario
liquid
índice de refracción
n20/D 1.4543 (lit.)
bp
75-77 °C/8 mmHg (lit.)
densidad
0.936 g/mL at 25 °C (lit.)
grupo funcional
amine
hydroxyl
cadena SMILES
CC(C)C(N)CO
InChI
1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3
Clave InChI
NWYYWIJOWOLJNR-UHFFFAOYSA-N
Aplicación
2-Amino-3-methyl-1-butanol was used in the synthesis of 1-allyl-2-pyrroleimines. It was also used as chiral nucleophile in the total synthesis of benanomicin-pradimicin antibiotics. It was used as homochiral guest compound during synthesis of crown ethers containing two chiral subunits.
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
194.0 °F - closed cup
Punto de inflamabilidad (°C)
90 °C - closed cup
Equipo de protección personal
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of organic chemistry, 73(21), 8376-8381 (2008-10-02)
1-Allyl-2-pyrroleimines obtained from (S)-valinol and (S)-phenylglycinol underwent highly diastereoselective addition of allylmagnesium chloride, used in excess amounts, to give the corresponding secondary amines with concomitant allyl to (Z)-1-propenyl isomerization of the 1-pyrrole substituent. Transformation of the 2-amino alcohol moiety to
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Earlier studies have indicated that sucrose increases 2-amino-3-methylimidazo[4,5-f]quinoline (IQ)-induced aberrant crypt foci in the colon. In this study, we investigated the role of sucrose in IQ-induced genotoxicity of the colon mucosa and liver. Big Blue rats were fed with IQ
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Certain functional analogs of amino acids were examined for their capacity to inhibit chemically induced expression of endogenous xenotropic retrovirus from Kirsten sarcoma virus transformed BALB/c (K-BALB) mouse cells. Partially synchronized cells cultured with aminoethylcysteine (AEC), parafluorophenylalanine (PFA), or valinol
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