16837-07-3

Basic information

• Product Name: 2-(4-BROMO-BUTOXY)-PHENOL
• Synonyms: 2-(4-BROMO-BUTOXY)-PHENOL
• CAS NO: 16837-07-3
• Molecular Formula: C₁₀H₁₃BrO₂
• Molecular Weight: 245.11
• Mol File: 16837-07-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-BROMO-BUTOXY)-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-BUTOXY)-PHENOL(16837-07-3)
• EPA Substance Registry System: 2-(4-BROMO-BUTOXY)-PHENOL(16837-07-3)

Safety Data

• Hazardous Substances Data: 16837-07-3(Hazardous Substances Data)

Usage

Category

Organic compound

Contains

Bromine atom, butoxy group

Usage

Precursor in organic synthesis, building block for pharmaceuticals, agrochemicals, and fine chemicals, manufacturing of dyes and pigments

Properties

Antimicrobial

Precautions

Harmful if ingested or inhaled, causes skin and eye irritation upon contact

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 7124-91-6 2,3,4,5-Tetrahydro-benzo[b][1,4]dioxocin 

Relevant articles and documents

Copper(I)-Catalyzed Interrupted Click Reaction: Synthesis of Diverse 5-Hetero-Functionalized Triazoles

The 5-heterofunctionalized triazoles are important scaffolds in bioactive compounds, but current click reactions (CuAAC) cannot produce these core structures. A copper(I)-catalyzed interrupted click reaction to access diverse 5-functionalized triazoles is reported. Various 5-amino-, thio-, and selenotriazoles were readily assembled in one step in high yields. The reaction proceeds under mild conditions with complete regioselectivity. It also features a broad substrate scope and good functional group compatibility.