7239-41-0

Basic information

• Product Name: 1-bromo-4-(4-bromobutoxy)butane
• Synonyms: 1-bromo-4-(4-bromobutoxy)butane
• CAS NO: 7239-41-0
• Molecular Formula: C₈H₁₆Br₂O
• Molecular Weight: 288.02
• Mol File: 7239-41-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 287.3°Cat760mmHg
• Flash Point: 114.8°C
• Appearance: /
• Density: 1.489g/cm³
• Vapor Pressure: 0.00433mmHg at 25°C
• Refractive Index: 1.494
• CAS DataBase Reference: 1-bromo-4-(4-bromobutoxy)butane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-4-(4-bromobutoxy)butane(7239-41-0)
• EPA Substance Registry System: 1-bromo-4-(4-bromobutoxy)butane(7239-41-0)

Safety Data

• Hazardous Substances Data: 7239-41-0(Hazardous Substances Data)

Usage

Brominated alkane

Yes

Butane backbone

Yes

Explanation

Different sources of media describe the Explanation of 7239-41-0 differently. You can refer to the following data:
1. The backbone of the molecule is a butane (C4H10) structure, which is a four-carbon chain.
2. A butoxy group is a butane molecule (C4H9) with one of the hydrogens replaced by an ethoxy (C2H5O) group. In this compound, the butoxy group is attached to the 4th carbon of the butane backbone.
3. 1-bromo-4-(4-bromobutoxy)butane is often used in organic synthesis, which is the study and construction of carbon-containing compounds.
4. This compound serves as a reagent in various chemical reactions due to its versatile properties.
5. 1-bromo-4-(4-bromobutoxy)butane is considered a hazardous substance, which means it poses potential health risks and should be handled with caution.

Number of bromine atoms

2

Butoxy group

Yes

Organic synthesis

Commonly used

Reagent in chemical reactions

Yes

Hazardous substance

Yes

InChI:InChI=1/C8H16Br2O/c9-5-1-3-7-11-8-4-2-6-10/h1-8H2

Upstream product

• 109-99-9 tetrahydrofuran 
• 507-19-7 t-butyl bromide 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 41138-92-5 methanesulfonyl bromide 
• 110-63-4 Butane-1,4-diol 
• 10035-10-6 hydrogen bromide 

Downstream Products

• 160982-13-8 (S)-3,4-dihydro-6-chloro-4-hydroxy-2-(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide 
• 88420-17-1 [4-acetyl-3-[4-[4-(4-acetyl-3-hydroxy-2-propylphenoxy)butoxy]butoxy]-2-propylphenoxy]acetic acid ethyl ester 
• 88419-92-5 [4-acetyl-3-[4-[4-(4-acetyl-3-hydroxy-2-propylphenoxy)butoxy]butoxy]-2-propylphenoxy]acetic acid 
• 110-52-1 1,4-dibromo-butane 
• 104835-66-7 {4-Acetyl-3-[4-(4-bromo-butoxy)-butoxy]-2-propyl-phenoxy}-acetic acid ethyl ester 
• 5392-06-3 6-oxa-undecanedinitrile 

Relevant articles and documents

Group 5 and group 6 metal halides as very efficient catalysts for acylative cleavage of ethers

Group 5 and 6 metal chlorides such as MoCl5, WCl6, NbCl5 and TaCl5 were found as very efficient catalysts for acylative cleavage of the C-O bond of ethers. Compared with conventional Lewis acid catalysts such as ZnCl2, AlCl3, SnCl4 and TiCl4, group 5 and 6 metal chlorides showed better results in the catalytic C-O bond cleavage of dibutyl ether with benzoyl chloride.