149557-17-5

Basic information

• Product Name: 1-bromo-3-propoxybenzene
• Synonyms: 1-bromo-3-propoxybenzene
• CAS NO: 149557-17-5
• Molecular Formula: C₉H₁₁BrO
• Molecular Weight: 215.08704
• Mol File: 149557-17-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-bromo-3-propoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-3-propoxybenzene(149557-17-5)
• EPA Substance Registry System: 1-bromo-3-propoxybenzene(149557-17-5)

Safety Data

• Hazardous Substances Data: 149557-17-5(Hazardous Substances Data)

Usage

Chemical structure

1-bromo-3-propoxybenzene consists of a benzene ring with a bromine atom (1-bromo) at the 1-position and a propoxy group (-OCH2CH2CH3) at the 3-position.

Physical state

It is a colorless to pale yellow liquid.

Odor

It has a slightly sweet odor.

Usage

Commonly used in organic synthesis and as an intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds.

Building block

Can be used as a building block in the synthesis of different functional molecules and materials.

Industrial application

Utilized in the production of polymers and plastics.

Hazardous nature

1-bromo-3-propoxybenzene is a hazardous chemical.

Safety precautions

Should be handled with caution due to its toxic and flammable properties.

Upstream product

• 89598-96-9 (3-bromophenyl)boronic acid 
• 71-23-8 propan-1-ol 
• 591-20-8 3-Bromophenol 
• 106-94-5 propyl bromide 

Relevant articles and documents

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The base mediated coupling of aliphatic alcohol pronucleophiles with unsymmetric diaryliodonium salt electrophiles is described. This metal-free reaction is operationally simple, proceeds at mild temperature, and displays broad substrate scope to generate industrially important alkyl-aryl ethers in moderate to excellent yield. The synthetic utility of these reactions is demonstrated, and aspects of sustainability are highlighted by the use of unsymmetric aryl(mesityl)iodonium arylating reagents.

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