749932-77-2

Usage

Chemical structure

1-(5-bromo-2-chlorophenyl)ethanol is a chemical compound with a phenyl ring containing a bromine and chlorine atom, and an alcohol functional group at one end of the molecule.

Functional groups

Contains a phenyl ring, a bromine atom, a chlorine atom, and an alcohol functional group.

Applications

Used in pharmaceutical and chemical synthesis, as a solvent, and as an intermediate in the production of other chemicals.

Reactivity

The presence of both bromine and chlorine atoms in its structure gives 1-(5-bromo-2-chlorophenyl)ethanol unique chemical properties and reactivity.

Industrial processes

Useful in a wide range of industrial processes due to its unique chemical properties and reactivity.

Solubility

As an alcohol derivative, it is likely soluble in water and other polar solvents, although specific solubility information is not provided in the material.

Boiling point

The boiling point is not provided in the material, but it can be inferred that the presence of bromine and chlorine atoms may increase the boiling point compared to similar compounds without these halogens.

Melting point

The melting point is not provided in the material, but it can be inferred that the presence of bromine and chlorine atoms may affect the melting point compared to similar compounds without these halogens.

Density

The density is not provided in the material, but it can be inferred that the presence of bromine and chlorine atoms may increase the density compared to similar compounds without these halogens.

Upstream product

• 917-54-4 methyllithium 
• 189628-37-3 2-chloro-5-bromobenzaldehyde 
• 105884-19-3 1-(2-bromo-5-chlorophenyl)ethan-1-one 

Downstream Products

• 105884-19-3 1-(2-bromo-5-chlorophenyl)ethan-1-one 
• 1126320-32-8 4-Bromo-1-chloro-2-(1-fluoro-ethyl)-benzene 

Relevant academic research and scientific papers

2-SUBSTITUTED-6-AMINO-5-ALKYL, ALKENYL OR ALKYNYL-4-PYRIMIDINECARBOXYLIC ACIDS AND 6-SUBSTITUTED-4-AMINO-3- ALKYL, ALKENYL OR ALKYNYL PICOLINIC ACIDS AND THEIR USE AS HERBICIDES

6-Amino-4-pyrimidinecarboxylic acids having alkyl, alkenyl or alkynyl substituents in the 5-position and 4-aminopicolinic acids having alkyl, alkenyl or alkynyl substituents in the 3-position, and their amine and acid derivatives, are potent herbicides demonstrating a broad spectrum of weed control.

2-(SUBSTITUTED PHENYL)-6-AMINO-5-ALKOXY, THIOALKOXY AND AMINOALKYL-4-PYRIMIDINECARBOXYLATES AND THEIR USE AS HERBICIDES

2-(Substituted phenyl)-6-amino-5-alkoxy, thioalkoxy and aminoalkyl-4-pyrimidinecarboxylic acid and its derivatives are potent herbicides demonstrating broad spectrum of weed control.

Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same

The invention relates to compounds of the formula 1 and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R1 and R2, are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula 1, and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula 1. The invention also relates to methods of preparing the compounds of formula 1.

INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME

The invention relates to compounds of the formula (I) and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R1and R2, are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula (I), and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula (I). The invention also relates to methods of preparing the compounds of formula (I).