123858-51-5

123858-51-5 - Names and Identifiers

Name	1-(2-amino-4-bromophenyl)ethanone
Synonyms	1-(2-Amino-4-bromophenyl) 1-(2-AMino-6-broMophenyl)ethanone 1-(2-amino-4-bromophenyl)ethanone 1-(2-Amino-4-bromophenyl)ethanone Ethanone, 1-(2-amino-4-bromophenyl)- ethanone, 1-(2-amino-4-bromophenyl)- 1-(2-amino-4-bromophenyl)ethan-1-one
CAS	123858-51-5
InChI	InChI=1/C8H8BrNO/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,10H2,1H3

123858-51-5 - Physico-chemical Properties

Molecular Formula	C8H8BrNO
Molar Mass	214.06
Density	1.535
Melting Point	82-84℃
Boling Point	322.9±27.0 °C(Predicted)
Flash Point	149.101°C
Vapor Presure	0mmHg at 25°C
pKa	1.23±0.10(Predicted)
Storage Condition	2-8°C(protect from light)
Refractive Index	1.608

123858-51-5 - Introduction

2 '-Amino -4'-bromoacetophenone, chemical formula C10H10BrNO, is an organic compound. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: 2 '-Amino -4'-bromoacetophenone is a solid, usually white or brown-yellow crystalline.
-Solubility: It is soluble in some organic solvents, such as alcohols and ethers, but insoluble in water.

Use:
-Chemical synthesis: 2 '-Amino -4'-bromoacetophenone can be used as a starting material or intermediate in organic synthesis for the synthesis of other organic compounds.
-Drug research: It also has certain applications in drug research and can be used as a functional group in drug molecules.

Preparation Method:
- 2 '-Amino -4'-bromoacetophenone is usually prepared by chemical synthesis. Acetophenone is usually used as a starting material, and an amino group and a bromo group are introduced in the reaction.
-The specific preparation method may vary according to actual needs and reaction conditions.

Safety Information:
-Due to the lack of specific safety assessment data, there is limited understanding of the toxicity and safety of 2 '-amino -4'-bromoacetophenone, so care should be taken when using it.
-When handling and storing 2 '-amino -4'-bromoacetophenone, take appropriate safety measures to avoid skin contact, inhalation or ingestion. Wear appropriate protective equipment such as gloves, goggles, etc.
-When using or handling this compound, it is best to follow laboratory safety procedures and follow relevant safety guidelines and regulations.

Last Update：2024-04-09 21:32:37