852110-51-1

Basic information

• Product Name: (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol
• Synonyms: (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol;7-bromo-2-hydroxymethyl-2,3-dihydrobenzo[b]furan
• CAS NO: 852110-51-1
• Molecular Formula: C₉H₉BrO₂
• Molecular Weight: 229.07056
• Mol File: 852110-51-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol(852110-51-1)
• EPA Substance Registry System: (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol(852110-51-1)

Safety Data

• Hazardous Substances Data: 852110-51-1(Hazardous Substances Data)

Usage

General Description

(7-Bromo-2,3-dihydrobenzofuran-2-yl)Methanol is a chemical compound with the molecular formula C9H9BrO2. It is a derivative of benzofuran, which is a heterocyclic compound with a fused benzene and furan ring system. (7-BroMo-2,3-dihydrobenzofuran-2-yl)Methanol is used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and organic molecules. It has the potential to exhibit biological activity and is of interest to researchers in the field of drug discovery. The bromo-substituted benzofuran moiety in this compound may confer unique properties and reactivity, making it a valuable intermediate in chemical synthesis. Overall, (7-Bromo-2,3-dihydrobenzofuran-2-yl)Methanol is a versatile and important chemical compound with potential applications in various fields of science and technology.

Upstream product

• 95-56-7 2-hydroxybromobenzene 
• 17269-81-7 2-bromo-6-(2-propenyl)phenol 
• 60333-75-7 O-allyl-2-bromophenol 

Downstream Products

• 852110-52-2 (7-bromo-2,3-dihydro-1-benzofuran-2-yl)methyl-4-methylbenzenesulfonate 

Relevant articles and documents

Green Organocatalytic Synthesis of Dihydrobenzofurans by Oxidation-Cyclization of Allylphenols

A green and cheap protocol for the synthesis of dihydrobenzofurans via an organocatalytic oxidation of o -allylphenols is presented. The use of 2,2,2-trifluoroacetophenone and H 2 O 2 as the oxidation system, leads to a highly useful synthetic method, where a variety of substituted o -allylphenols were cyclized in high yields..

MACROCYCLIC GHRELIN RECEPTOR MODULATORS AND METHODS OF USING THE SAME

The present invention provides novel conformationally-defined macrocyclic compounds that can function as selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, bone disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.

DIHYDROBENZOFURAN COMPOUNDS AND USES THEREOF

Dihydrobenzofuran compounds of Formula (I), including salts, prodrugs, hydrates and solvates thereof, that act as 5-HT2 receptor ligands and their uses in the treatment of diseases linked to the activation of 5-HT2 receptors in anima