188011-21-4

Basic information

• Product Name: 1-(bromomethyl)-3,5-bis(octyloxy)benzene
• Synonyms: 1-(bromomethyl)-3,5-bis(octyloxy)benzene
• CAS NO: 188011-21-4
• Molecular Weight: 427.465
• Mol File: 188011-21-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 487.9±30.0 °C(Predicted)
• Density: 1.073±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(bromomethyl)-3,5-bis(octyloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(bromomethyl)-3,5-bis(octyloxy)benzene(188011-21-4)
• EPA Substance Registry System: 1-(bromomethyl)-3,5-bis(octyloxy)benzene(188011-21-4)

Safety Data

• Hazardous Substances Data: 188011-21-4(Hazardous Substances Data)

Usage

Chemical structure

1-(bromomethyl)-3,5-bis(octyloxy)benzene consists of a benzene ring with two octyloxy (C8H17O-) groups attached at positions 3 and 5, and a bromomethyl (-CH2Br) group attached at position 1.

Building block

It is commonly used as a building block in the synthesis of various organic compounds.

Application

It is particularly used in the field of materials science and organic electronics.

Solubility

The octyloxy groups make it highly soluble in nonpolar organic solvents.

Reactivity

The bromomethyl group makes it reactive towards various nucleophiles.

Preparation

It is useful for the preparation of functionalized benzene derivatives.

Intermediate

Its unique structure and reactivity make it a valuable intermediate for the production of polymers, liquid crystals, and organic semiconductors.

Upstream product

• 87963-84-6 methyl 3,5-bis(octyloxy)benzoate 
• 111-83-1 1-bromo-octane 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 188011-20-3 1-(hydroxymethyl)-3,5-bis(octyloxy)benzene 

Downstream Products

• 188011-23-6 3,5-bis[3,5-bis(octyloxy)phenylmethyloxy]benzyl alcohol 
• 1338348-50-7 diethyl 3,5-bis(octyloxy)benzylphosphonate 
• 1338348-52-9 (E)-4-(3,5-bis(octyloxy)styryl)phenol 
• 1233495-66-3 C₃₀H₄₄O₅ 
• 255827-68-0 {4-[(2S,3R)-3-(3,5-Bis-octyloxy-benzyloxy)-2-(3,5-bis-octyloxy-benzyloxymethyl)-butyl]-phenyl}-methanol 
• 255827-67-9 {4-[(2S,3R)-3-(3,5-Bis-octyloxy-benzyloxy)-2-(3,5-bis-octyloxy-benzyloxymethyl)-butyl]-benzyloxy}-tert-butyl-diphenyl-silane 

Relevant articles and documents

Construction of Janus dendrimers through a self-assembly approach involving chiral discrimination at a focal point

A strategy to build Janus dendrimersviathe chirality-directed self-assembly of heteroleptic Zn(ii) BOX complexes is reported. The method allows quantitative synthesis of Janus dendrimersin situwithout the need for purifications. Each dendritic domain of t

Synthesis and properties of new, spatially relaxed dendrons containing internal carboxyl groups

We synthesized a series of new dendrons with up to fourteen internal carboxyl groups. These dendrons are made from a branching unit and a spacer unit with a carboxyl group. The growth reactions (formation of the benzylic ether bonds) are completed within