123858-51-5
1-(2-amino-4-bromophenyl)ethanone
CAS: 123858-51-5
Molecular Formula: C8H8BrNO
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.
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
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View History
123858-51-5
Bromobithiophenecarboxaldehyde
氮螺溴酸盐
171596-43-3
1092460-79-1
1326241-13-7
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Bromobithiophenecarboxaldehyde
氮螺溴酸盐
171596-43-3
1092460-79-1
1326241-13-7
121343-82-6
914651-17-5
866872-31-3
13236-02-7