3-Bromo-2-butanol is an organic compound characterized by the presence of a bromine atom and a hydroxyl group (-OH) attached to a butane backbone. It is classified as a secondary alcohol due to the hydroxyl group being bonded to a carbon atom that is connected to two other carbon atoms. The molecular formula for 3-bromo-2-butanol is C4H9BrO, indicating that it contains four carbon atoms, nine hydrogen atoms, one bromine atom, and one oxygen atom. This compound typically appears as a colorless to pale yellow liquid and has a moderate boiling point, reflecting its molecular structure. It is soluble in water due to the polar nature of the hydroxyl group, while the bromine substituent can influence its reactivity, making it a useful intermediate in organic synthesis. 3-Bromo-2-butanol can participate in various chemical reactions, including nucleophilic substitutions and eliminations, and is often utilized in the synthesis of more complex organic molecules.

3-Bromo-2-butanol

5798-80-1: 3-Bromo-2-butanol is an organic compound characterized by the presence of a bromine atom and a hydroxyl group (-OH) attached to a butane backbone. It is classified as a secondary alcohol due to the hydroxyl group being bonded to a carbon atom that is connected to two other carbon atoms. The molecular formula for 3-bromo-2-butanol is C4H9BrO, indicating that it contains four carbon atoms, nine hydrogen atoms, one bromine atom, and one oxygen atom. This compound typically appears as a colorless to pale yellow liquid and has a moderate boiling point, reflecting its molecular structure. It is soluble in water due to the polar nature of the hydroxyl group, while the bromine substituent can influence its reactivity, making it a useful intermediate in organic synthesis. 3-Bromo-2-butanol can participate in various chemical reactions, including nucleophilic substitutions and eliminations, and is often utilized in the synthesis of more complex organic molecules.

<p>3-Bromobutan-2-ol is an alcohol that is used as a chemical intermediate in the preparation of bromohydrins, which are intermediates in the production of other organic compounds. 3-Bromobutan-2-ol can be prepared by catalytic asymmetric synthesis from 2-bromoethanol and dimethylamine. The stereoisomers of 3-bromobutan-2-ol are optically active and can be separated by column chromatography or recrystallization. The synthetic route for this compound involves esterification with formic acid followed by hydrolysis to give 3-bromobutanone, which then undergoes a dehydration reaction with boron tribromide to produce 3-bromobutan-2-ol. This product has been shown to have antifungal properties against Candida albicans, Coccidioides immitis, and Aspergillus fumigatus</p>

CAS 5798-80-1

3-Bromo-2-butanol

3-Bromobutan-2-ol

Ref: 3D-FAA79880