(R)-3-amino-1-butanol CAS: 61477-40-5
Catalog Number | XD94350 |
Product Name | (R)-3-amino-1-butanol |
CAS | 61477-40-5 |
Molecular Formula | C4H11NO |
Molecular Weight | 89.14 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(R)-3-amino-1-butanol, also known as (R)-3-aminobutanol or (R)-1-amino-3-butanol, is a chiral compound with important applications in the pharmaceutical and chemical industries. Its unique structure and properties make it an essential building block for the synthesis of various compounds.One notable use of (R)-3-amino-1-butanol is in the production of pharmaceutical drugs. It serves as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and can be used to create a range of pharmaceutical compounds. By incorporating (R)-3-amino-1-butanol into the synthesis process, chemists can introduce chirality, or the arrangement of atoms in a molecule, which is crucial for achieving the desired biological activity and potency in many drugs. This compound has been employed in the synthesis of drugs such as antivirals, antineoplastics, beta blockers, and anti-epileptics.Additionally, (R)-3-amino-1-butanol is utilized for the creation of chiral ligands, which are essential components in asymmetric catalysis. Asymmetric catalysis is a highly valuable technique that enables chemists to selectively produce a desired stereoisomer of a compound. These chiral ligands, when coupled with transition metal catalysts, facilitate asymmetric transformations, leading to the production of enantiomerically pure compounds. (R)-3-amino-1-butanol has been employed in the synthesis of chiral ligands used in reactions such as asymmetric hydrogenation and asymmetric allylation.Moreover, (R)-3-amino-1-butanol finds applications in the manufacturing of agrochemicals and fine chemicals. It can be used as a precursor for the synthesis of various compounds, including herbicides, insecticides, and flavors. By incorporating (R)-3-amino-1-butanol into the synthesis process, chemists can introduce chirality to these compounds, which can enhance their biological activity, specificity, and environmental impact.It is important to note that (R)-3-amino-1-butanol should be handled with care as it is a flammable liquid and can cause irritation to the skin and eyes. It should be stored in a cool, well-ventilated area away from heat and incompatible materials.In conclusion, (R)-3-amino-1-butanol is a versatile compound with wide applications in the pharmaceutical and chemical industries. Its incorporation in drug synthesis enables the production of enantiomerically pure compounds with desired biological activities. Furthermore, its use in the production of chiral ligands for asymmetric catalysis allows for the selective synthesis of desired stereoisomers. Additionally, (R)-3-amino-1-butanol plays a crucial role in the synthesis of agrochemicals, facilitating the production of chirally pure compounds with enhanced properties.