Product Name:3-Amino-3-(2-bromophenyl)oxetane hydrochloride

IUPAC Name:3-(2-bromophenyl)oxetan-3-amine hydrochloride

CAS:1416323-20-0
Molecular Formula:C9H11BrClNO
Purity:95%+
Catalog Number:CM291861
Molecular Weight:264.55

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Product Details

CAS NO:1416323-20-0
Molecular Formula:C9H11BrClNO
Melting Point:-
Smiles Code:BrC1=CC=CC=C1C2(N)COC2.[H]Cl
Density:
Catalog Number:CM291861
Molecular Weight:264.55
Boiling Point:
MDL No:MFCD22628717
Storage:

Category Infos

Oxetanes
Oxygen heterocycles are one of the most common heterocycles in drugs and natural products. Oxetene has high polarity and is also a good acceptor for hydrogen bond, which contributes to the metabolism and chemical stability of its host molecules. When substituted for commonly used functional groups such as gem dimethyl or carbonyl, oxetane units can induce profound changes in water solubility, lipophilicity, metabolic stability and conformational preference. Four of the FDA-approved drugs contain oxetenes: Orlistat, Paclitaxel, and two of its derivatives, Docetaxel and Cabazitaxel. Currently, oxetane-containing building blocks are flourishing in medicinal chemistry and drug discovery.

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Product Other Information

Product Overview 3-Amino-3-(2-bromophenyl)oxetane hydrochloride, also known as ABOH, is a chemical compound that has a wide range of applications in scientific research. It is a versatile compound that can be used in a variety of fields, including organic synthesis, biochemistry, and pharmacology. ABOH is a brominated amine derivative of oxetane and can be synthesized from 3-bromo-2-hydroxybenzaldehyde and ethylamine.
Synthesis and Application 3-Amino-3-(2-bromophenyl)oxetane hydrochloride can be synthesized from 3-bromo-2-hydroxybenzaldehyde and ethylamine. The reaction begins with the condensation of the two reactants in the presence of a strong base, such as sodium or potassium hydroxide. The product of this reaction is an aldehyde-amine adduct, which is then reacted with hydrochloric acid to yield 3-Amino-3-(2-bromophenyl)oxetane hydrochloride. The reaction can be carried out at room temperature and has a high yield of 3-Amino-3-(2-bromophenyl)oxetane hydrochloride. 3-Amino-3-(2-bromophenyl)oxetane hydrochloride has a wide range of applications in scientific research. It is used as a reagent in organic synthesis, as it can be used to synthesize a variety of compounds. 3-Amino-3-(2-bromophenyl)oxetane hydrochloride has also been used in biochemistry, as it can be used to study the structure and function of proteins. In pharmacology, 3-Amino-3-(2-bromophenyl)oxetane hydrochloride has been used to study the structure and function of drugs.
Future Directions There are several potential future directions for 3-Amino-3-(2-bromophenyl)oxetane hydrochloride. It could be used to study the structure and function of proteins or to study the structure and function of drugs. In addition, it could be used to develop new and improved drugs or to develop new methods of drug delivery.