Nombre del producto:(R)-3-aminobutan-1-ol

IUPAC Name:(3R)-3-aminobutan-1-ol

CAS:61477-40-5
Fórmula molecular:C4H11NO
Pureza:97%
Número de catálogo:CM108315
Peso molecular:89.14

Unidad de embalaje Stock disponible Precio($) Cantidad
CM108315-100g in stock ijǭ
CM108315-500g in stock ţŁij

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :61477-40-5
Fórmula molecular:C4H11NO
Punto de fusión:-
Código de sonrisas:C[C@@H](N)CCO
Densidad:
Número de catálogo:CM108315
Peso molecular:89.14
Punto de ebullición:168°C at 760 mmHg
Nº Mdl:MFCD13184351
Almacenamiento:Keep in dark place, store at 2-8°C.

Category Infos

Aliphatic Chain Compounds
Aliphatic chain compounds include aliphatic compounds and chain compounds containing other elements or groups. Aliphatic hydrocarbons are hydrocarbons with the basic properties of aliphatic compounds. In aliphatic compounds, carbon atoms are arranged in straight chain, branched chain or cyclic, which are respectively called straight chain aliphatic hydrocarbons, branched chain aliphatic hydrocarbons and alicyclic hydrocarbons. Some cyclic hydrocarbons are different in nature from aromatic hydrocarbons, and are very similar to aliphatic hydrocarbons. Such cyclic hydrocarbons are called alicyclic hydrocarbons. In this way, aliphatic hydrocarbons become a general term for all hydrocarbons except aromatic hydrocarbons. Aliphatic hydrocarbons and their derivatives (including halogenated hydrocarbons) and alicyclic hydrocarbons and their derivatives are collectively referred to as aliphatic compounds.

Column Infos

Alcohols
Alcohol is a type of organic compound that carries at least one hydroxyl ( −OH) functional group bound to a saturated carbon atom.

Related Products



Product Other Information

Product Overview (R)-3-aminobutan-1-ol, also known as (R)-1-amino-3-butyrolactam, is an organic compound that is commonly used in scientific research. It is a colorless liquid with a faint odor, and it is soluble in water and other organic solvents. As a chiral molecule, (R)-3-aminobutan-1-ol has two enantiomers, (R)- and (S)-, which differ in their physical and chemical properties. (R)-3-aminobutan-1-ol has a variety of applications in scientific research, including synthesis, catalysis, and drug discovery.
Synthesis and Application (R)-3-aminobutan-1-ol can be synthesized through a variety of methods, including chemical synthesis, enzymatic synthesis, and biotransformation. In chemical synthesis, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and a base, such as sodium hydroxide. In enzymatic synthesis, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and an enzyme, such as a lipase or esterase. In biotransformation, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and a microorganism, such as a bacterium or fungus. (R)-3-aminobutan-1-ol has a variety of applications in scientific research, including synthesis, catalysis, and drug discovery. In synthesis, (R)-3-aminobutan-1-ol is used as a starting material in the synthesis of various compounds, including drugs, dyes, and polymers. In catalysis, (R)-3-aminobutan-1-ol is used as a catalyst in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and fragrances. In drug discovery, (R)-3-aminobutan-1-ol is used as a starting material in the synthesis of various drugs, including antibiotics, anti-cancer drugs, and anti-inflammatory drugs.
Future Directions The future directions of (R)-3-aminobutan-1-ol research include further exploration of its biochemical and physiological effects, further exploration of its mechanism of action, further exploration of its use in drug discovery, and further exploration of its use in the synthesis of various compounds. In addition, further research is needed to determine the safety and efficacy of (R)-3-aminobutan-1-ol in humans.