1114808-93-3

Basic information

• Product Name: 1-BENZYLOXY-5-BROMO-2-METHYLBENZENE
• Synonyms: 1-BENZYLOXY-5-BROMO-2-METHYLBENZENE;2-Benzyloxy-4-bromo-1-methylbenzene;2-Benzyloxy-4-bromotoluene
• CAS NO: 1114808-93-3
• Molecular Formula: C₁₄H₁₃BrO
• Molecular Weight: 277.15642
• Mol File: 1114808-93-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 1-BENZYLOXY-5-BROMO-2-METHYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZYLOXY-5-BROMO-2-METHYLBENZENE(1114808-93-3)
• EPA Substance Registry System: 1-BENZYLOXY-5-BROMO-2-METHYLBENZENE(1114808-93-3)

Safety Data

• Hazardous Substances Data: 1114808-93-3(Hazardous Substances Data)

Usage

Structure

Benzene derivative with a bromine atom, a methyl group, and a benzyloxy group attached to the benzene ring

Applications

a. Organic synthesis
b. Chemical research
c. Building block for pharmaceuticals, agrochemicals, and other organic compounds
d. Development of new materials and specialty chemicals

Significance

a. Versatile compound
b. Valuable for creating functionalized molecules
c. Diverse applications in pharmaceutical and chemical industries

Potential

Significant potential for use in various fields of research and industry

Upstream product

• 36138-76-8 5-bromo-2-methylphenol 
• 100-39-0 benzyl bromide 

Downstream Products

• 1687-65-6 2-methyl,5-ethyl-phenol 
• 1638631-78-3 3-benzyloxy-N-(3-methoxyphenyl)-4-methylaniline 
• 1638631-80-7 2-benzyloxy-7-methoxycarbazole-3-carbaldehyde 
• 1021685-17-5 2-(benzyloxy)-7-methoxy-3-methyl-9H-carbazole 
• 1638631-79-4 2-benzyloxy-5-methoxy-3-methylcarbazole 
• 119736-83-3 2-hydroxy-3-formyl-7-methoxycarbazole 
• 1407543-42-3 C₂₆H₂₉ClO₂ 
• 1407543-41-2 C₂₀H₂₇O₅P 
• 1407543-40-1 C₁₇H₂₀O₃ 

Relevant articles and documents

Diastereoselective Intramolecular Heck Reaction Assisted by an Acetate Group: Synthesis of the Decahydrobenzofluorene Derivative Dasyscyphin e

The first synthesis of antifungal sesquiterpene quinol dasyscyphin E was achieved starting from trans-communic acid. The process described involves the first diastereoselective synthesis of this type of compound by cyclization of an aryl bicyclosesquiterpene. The acid was efficiently transformed into a sesquiterpene synthon, which was converted into the corresponding bromoaryl sesquiterpene. The key step of synthetic sequence was the cyclization of the latter under Heck reaction conditions, which yielded the tetracyclic skeleton of the target compound with complete diastereoselectivity. The participation of an acetate group is decisive, both for the course of the Heck reaction and for the stereoselectivity of the process.

2,5-DIALKYL-4-H/HALO/ETHER-PHENOL COMPOUNDS

The present disclosure provides phenolic compounds useful in the treatment of neurological conditions such as convulsions and tremors, having the structure of Formula (I): wherein R2, R4, and R5, are as defined in the detailed description; pharmaceutical compositions comprising at least one of the compounds; and methods for treating neurological conditions.

FLASH AND GLOW 1,2-DIOXETANES

Compounds having chemiluminescent flash and glow properties. Also disclosed are methods using the compounds to generate light, detect and/or quantify enzymes, antigens, and/or nucleic acids. Also disclosed are kits relating to these compounds.