22589-50-0

Basic information

• Product Name: 4'-AMINO-3',5'-DIBROMOACETOPHENONE
• Synonyms: 4'-AMINO-3',5'-DIBROMOACETOPHENONE;4'-Amino-3',5'-dibromoacetophenone;1-(4-Amino-3,5-dibromo-phenyl)-ethanone;1-(4-Amino-3,5-dibromophenyl)ethan-1-one
• CAS NO: 22589-50-0
• Molecular Formula: C₈H₇Br₂NO
• Molecular Weight: 292.96
• Mol File: 22589-50-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 4'-AMINO-3',5'-DIBROMOACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-AMINO-3',5'-DIBROMOACETOPHENONE(22589-50-0)
• EPA Substance Registry System: 4'-AMINO-3',5'-DIBROMOACETOPHENONE(22589-50-0)

Safety Data

• Hazardous Substances Data: 22589-50-0(Hazardous Substances Data)

Usage

General Description

4'-Amino-3',5'-dibromoacetophenone is a chemical compound with the molecular formula C8H7Br2NO. It is a yellow solid with a molecular weight of 274.96 g/mol. 4'-AMINO-3',5'-DIBROMOACETOPHENONE is often used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It has a wide range of applications in the pharmaceutical and chemical industries, particularly in the development of new drugs and medications. It is also used as a reagent in organic synthesis and as a building block for the production of other chemical compounds. Additionally, 4'-amino-3',5'-dibromoacetophenone has potential uses in research and development, as well as in the manufacturing of specialty chemicals.

Upstream product

• 7726-95-6 bromine 
• 99-92-3 p-aminobenzophenone 
• 64-19-7 acetic acid 
• 107-21-1 ethylene glycol 

Downstream Products

• 14401-73-1 3,5-dibromoacetophenone 
• 6311-60-0 3,5-dibromonitrobenzene 
• 84483-37-4 2,6-dibromo-4,N-dinitro-aniline 
• 30095-55-7 4'-amino-2,3',5'-tribromoacetophenone 
• 60677-25-0 3,5-dibromo-4-methoxycarbonylamino-α-bromoacetophenone 
• 60677-64-7 3,5-dibromo-4-methoxycarbonylamino-α-(tert-butylaminomethyl)benzyl alcohol 
• 535992-33-7 1-(3,5-dibromo-2-nitro-phenyl)-ethanone 
• 87976-31-6 C₇H₃⁽²⁾H₃O₂ 
• 116772-89-5 C₈H₃⁽²⁾H₇O 
• 116772-87-3 C₈H₄⁽²⁾H₆O 
• 104892-58-2 3,4,5-tribromoacetophenone 
• 37960-84-2 [3,5-D₂]benzoic acid 
• 56340-97-7 2-Amino-5-[2-(2-benzo[1,3]dioxol-5-yl-1-methyl-ethylamino)-acetyl]-isophthalonitrile 
• 97760-71-9 1-(4'-Amino-3',5'-dicyano-phenyl)-2-tert-butylamino-ethanol 

Relevant articles and documents

Phenylethanolamine β receptor agonist synthetic method

The invention discloses a phenylethanolamine β receptor agonist synthetic method, comprises the following steps: S1: the 4 - amino acetophenone dissolved in an organic solvent, with the electrophilic reagent occurs on the benzene ring substituted halogenated reaction, generating [...] intermediate; [...] intermediates in organic solvent or in water, under the catalysis of the metal catalyst with the cyanide reagent undergo nucleophilic substitution reaction, generating phenyl ketone intermediate; S2: phenyl ketone intermediates in organic solvent, with the copper bromide generating carbonyl α bromo reaction to produce α - bromoacetophenone intermediates; S3: α - bromoacetophenone intermediates in organic solvent with tert-butyl amine or isopropylamine reaction intermediates acetophenone amines; S4: acetophenone amine intermediates in organic solvent, with the reduction hydrogenation reagent react to generate the phenylethanolamine β receptor agonists; synthetic method of this invention a simple and highly efficient and cheap and easy to obtain, atom utilization is high, the synthetic product chemical purity is greater than 99%, to meet the detection requirements of the food safety.