7239-41-0

Usage

Brominated alkane

Yes

Butane backbone

Yes

Explanation

The backbone of the molecule is a butane (C4H10) structure, which is a four-carbon chain.

Explanation

A butoxy group is a butane molecule (C4H9) with one of the hydrogens replaced by an ethoxy (C2H5O) group. In 1-bromo-4-(4-bromobutoxy)butane, the butoxy group is attached to the 4th carbon of the butane backbone.

Explanation

1-bromo-4-(4-bromobutoxy)butane is often used in organic synthesis, which is the study and construction of carbon-containing compounds.

Explanation

1-bromo-4-(4-bromobutoxy)butane serves as a reagent in various chemical reactions due to its versatile properties.

Explanation

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

• 5392-06-3 6-oxa-undecanedinitrile 
• 104835-66-7 {4-Acetyl-3-[4-(4-bromo-butoxy)-butoxy]-2-propyl-phenoxy}-acetic acid ethyl ester 
• 110-52-1 1,4-dibromo-butane 
• 88419-92-5 [4-acetyl-3-[4-[4-(4-acetyl-3-hydroxy-2-propylphenoxy)butoxy]butoxy]-2-propylphenoxy]acetic acid 
• 88420-17-1 [4-acetyl-3-[4-[4-(4-acetyl-3-hydroxy-2-propylphenoxy)butoxy]butoxy]-2-propylphenoxy]acetic acid ethyl ester 
• 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 

Relevant academic research and scientific papers

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.

Metal-assisted Reactions. Part 17. Ring-opening and Dimerization of Cyclic Ethers by Titanium Halides

Reaction of TiCl4 or TiBr4 with a variety of cyclic ethers gives, predominantly, products resulting from simple ring-opening or from ring-opening with simultaneous condensation to dimeric species.The variations in yields of these two kinds of products might be correlated qualitatively with an initial formation of the complex TiX4*2E (X = Cl or Br; E = cyclic ether) in which the ethers were held in a cis or trans relationship.Although such a correlation might suggest that TiCl4 but not TiBr4 exerts a template effect on the condensation, stereochemical considerations of the reaction products indicate otherwise.TiCl3 and VCl3 do not give similar results and TiF4 gives no reaction.