2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride
2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride
CAS: 41995-19-1
Molecular Formula: C8H7Cl2NO.HCl
2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride - Names and Identifiers
| Name | 2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride |
| Synonyms | 2-Amino-3',4'-dichloroacetophenone HCl 2-(3,4-dichlorophenyl)-2-oxoethanaminium chloride 2-(3,4-DICHLOROPHENYL)-2-OXOETHYLAMINE HYDROCHLORIDE 2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride 2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride 2-aMino-1-(3,4-dichlorophenyl)ethan-1-one hydrochloride |
| CAS | 41995-19-1 |
| InChI | InChI=1/C8H7Cl2NO.ClH/c9-6-2-1-5(3-7(6)10)8(12)4-11;/h1-3H,4,11H2;1H |
2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride - Physico-chemical Properties
| Molecular Formula | C8H7Cl2NO.HCl |
| Molar Mass | 240.51 |
| Boling Point | 371.9°C at 760 mmHg |
| Flash Point | 178.7°C |
| Vapor Presure | 6.83E-06mmHg at 25°C |
2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride - Introduction
2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride is a compound with the formula C8H8Cl2NO · HCl. It is a white solid powder with a special smell.
The main use of this compound is as an intermediate in organic synthesis. It can be used to synthesize various organic compounds, such as drugs, pesticides and dyes.
The preparation method of 2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride can be obtained by the reaction of chloroacetophenone and chlorine dioxide. First, chloroacetophenone is reacted with chlorine dioxide under basic conditions to produce 2-(3,4-dichlorophenyl)-2-oxoacetic acid. This acid is then reacted with hydrogen chloride to give 2-(3,4-dichlorophenyl)-2-oxoethylamine hydrochloride.
Regarding safety information, appropriate safety measures need to be taken during storage and handling of this compound. It is a combustible solid that may cause a fire when exposed to high temperatures or open flames. During the operation, care should be taken to avoid contact with skin, eyes and mucous membranes. In case of skin contact, rinse immediately with plenty of water. If ingested or inhaled, seek medical attention immediately. During storage, it should be stored in a dry and ventilated place, away from fire and oxidizing agents.
The main use of this compound is as an intermediate in organic synthesis. It can be used to synthesize various organic compounds, such as drugs, pesticides and dyes.
The preparation method of 2-(3,4-Dichlorophenyl)-2-oxoethylamine hydrochloride can be obtained by the reaction of chloroacetophenone and chlorine dioxide. First, chloroacetophenone is reacted with chlorine dioxide under basic conditions to produce 2-(3,4-dichlorophenyl)-2-oxoacetic acid. This acid is then reacted with hydrogen chloride to give 2-(3,4-dichlorophenyl)-2-oxoethylamine hydrochloride.
Regarding safety information, appropriate safety measures need to be taken during storage and handling of this compound. It is a combustible solid that may cause a fire when exposed to high temperatures or open flames. During the operation, care should be taken to avoid contact with skin, eyes and mucous membranes. In case of skin contact, rinse immediately with plenty of water. If ingested or inhaled, seek medical attention immediately. During storage, it should be stored in a dry and ventilated place, away from fire and oxidizing agents.
Last Update：2024-04-09 21:01:54
Supplier List
View History
2-Amino-1-(3,4-dichlorophenyl)ethanone hydrochloride
Sodium chloride crystal optic rectangle, 30mm x 15mm x 4mm, unpolished
2,6-DIMETHOXY-N-(4-METHOXYPHENYL)BENZAMIDE
四氢吡咯
N2-[(苄氧基)羰基]-N-(三苯基甲基)-D-天冬氨酰胺
sodium 6-tert-butyl-4-ethoxynicotinate
2-(3,5-二碘-4-氧代-1-吡啶基)乙酸
2-(4-broMo-3-Methoxyphenyl)acetonitrile
2,2-二甲氧基-1,6-二氮杂-2-硅杂辛烷
2'-溴-2-苯基螺[9H-芴-9,9'-[9H]氧杂蒽]
Sodium chloride crystal optic rectangle, 30mm x 15mm x 4mm, unpolished
2,6-DIMETHOXY-N-(4-METHOXYPHENYL)BENZAMIDE
四氢吡咯
N2-[(苄氧基)羰基]-N-(三苯基甲基)-D-天冬氨酰胺
sodium 6-tert-butyl-4-ethoxynicotinate
2-(3,5-二碘-4-氧代-1-吡啶基)乙酸
2-(4-broMo-3-Methoxyphenyl)acetonitrile
2,2-二甲氧基-1,6-二氮杂-2-硅杂辛烷
2'-溴-2-苯基螺[9H-芴-9,9'-[9H]氧杂蒽]