1849-76-9

Usage

Uses

Used in Pharmaceutical Industry:
AKOS B028976 is used as a pharmaceutical compound for its potential biological and medicinal properties. Its interactions with certain proteins and enzymes in biological systems make it a promising candidate for the development of new therapeutic agents.
AKOS B028976 is used as a research tool for studying its pharmacological and physiological effects, which can help in the discovery and development of new drugs for various diseases and disorders.
AKOS B028976 is also used in drug discovery and development processes, where its specific chemical structure and interactions with biological targets can be leveraged to design and optimize new therapeutic agents with improved efficacy and safety profiles.

InChI:InChI=1/C7H4BrClO2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H

Upstream product

• 2420-16-8 4-hydroxy-3-chlorobenzaldehyde 
• 67-56-1 methanol 
• 57018-10-7 2-bromo-6-chloro-4-methylphenol 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 161565-36-2 3-bromo-5-chloro-4-methoxybenzaldehyde 
• 511295-15-1 5'-chloro-2'-[2-(3'-chloro-5'-[1,3]dioxan-2-yl-6,2'-dimethoxy-biphenyl-3-yl)-ethyl]-2,4'-dimethoxy-biphenyl-4-carboxylic acid methyl ester 
• 511295-14-0 2'-[2-(3'-chloro-5'-[1,3]dioxan-2-yl-6,2'-dimethoxy-biphenyl-3-yl)-ethyl]-2,4'-dimethoxy-biphenyl-4-carboxylic acid methyl ester 
• 511295-18-4 5-chloro-5'-[2-(5-chloro-4'-hydroxymethyl-4,2'-dimethoxy-biphenyl-2-yl)-ethyl]-6,2'-dimethoxy-biphenyl-3-carbaldehyde 
• 511295-17-3 5-chloro-5'-[2-(4'-hydroxymethyl-4,2'-dimethoxy-biphenyl-2-yl)-ethyl]-6,2'-dimethoxy-biphenyl-3-carbaldehyde 
• 511295-24-2 5-Chloro-5'-[2-(4'-formyl-4,2'-dimethoxy-biphenyl-2-yl)-ethyl]-6,2'-dimethoxy-biphenyl-3-carbaldehyde 
• 511295-07-1 2-(3-bromo-5-chloro-4-methoxyphenyl)-1,3-dioxane 

Relevant academic research and scientific papers

Syntheses of chlorinated bisbibenzyls from bryophytes

Chlorinated bisbibenzyls of the isoplagiochin type detected in different bryophyte species were synthesized by an efficient and flexible unit construction system making extensive use of Suzuki and Wittig protocols.

Phenolic oxidation of o,o'-dihalogenated phenols

A detailed inspection of phenolic oxidation products derived from the o,o'-dihalogenated cresol derivatives (1a - 1e) indicated that the bromo and chloro substituents promoted the oxidation leading to the corresponding diaryl ethers, whereas the iodo derivatives provided the diaryls. Selective reduction of 6d and its tyrosine derivative afforded the corresponding diaryl ethers carrying two chlorine atoms (14, 15). Interpretation of the selectivity of the phenolic oxidation was attempted by employing theoretical calculations.