7131-09-1

Basic information

• Product Name: p-(1-AdaMantyl)benzyl broMide
• Synonyms: p-(1-AdaMantyl)benzyl broMide
• CAS NO: 7131-09-1
• Molecular Formula: C₁₇H₂₁Br
• Molecular Weight: 305.25264
• Mol File: 7131-09-1.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: p-(1-AdaMantyl)benzyl broMide(CAS DataBase Reference)
• NIST Chemistry Reference: p-(1-AdaMantyl)benzyl broMide(7131-09-1)
• EPA Substance Registry System: p-(1-AdaMantyl)benzyl broMide(7131-09-1)

Safety Data

• Hazardous Substances Data: 7131-09-1(Hazardous Substances Data)

Upstream product

• 1459-55-8 4-(1-adamantyl)toluene 
• 7163-95-3 4-(adamantan-1-yl)benzonitrile 
• 1459-49-0 1-(4-nitrophenyl)adamantane 
• 780-68-7 1-phenyladamantane 
• 1459-48-9 4-(tricyclo[3.3.1.1^3,7]dec-1-yl)aniline 
• 7123-78-6 4-(adamant-1-yl)benzoic acid 
• 7164-55-8 ethyl 4-(adamantan-1-yl)benzoate 
• 768-95-6 1-adamanthanol 
• 768-90-1 1-Adamantyl bromide 
• 108-88-3 toluene 

Downstream Products

• 117077-34-6 4-(1-adamantyl)phenylacetonitrile 
• 911838-00-1 2-[4-(1-adamantyl)benzylsulfanyl]-6-methyl-pyrimidin-4(3H)-one 
• 117118-92-0 2-(4-Adamantan-1-yl-phenyl)-ethylamine; hydrochloride 
• 117141-35-2 N-[2-(4-Adamantan-1-yl-phenyl)-ethyl]-2-chloro-acetamidine; hydrochloride 
• 7131-08-0 (4-(adamantan-1-yl)phenyl)methanol 

Relevant articles and documents

Preparation and application of thiosemicarbazone compound

The invention discloses a thiosemicarbazone compound, and biological activity analysis is carried out on the thiosemicarbazone compound. The invention also discloses application of the thiosemicarbazone compound in preparation of antibacterial drugs. According to the invention, important intermediates 6a-6h are synthesized from hydrazine hydrate and react with adamantane benzaldehyde respectivelyto synthesize eight adamantane aromatic aldehyde thiosemicarbazone compounds, the structures of the compounds can be confirmed by infrared, nuclear magnetic hydrogen spectrum, carbon spectrum and massspectrum methods, and the antibacterial activity of the compounds is tested in vitro. The result shows that the compound has a good antibacterial effect on escherichia coli and bacillus subtilis.

Modes of Micromolar Host-Guest Binding of β-Cyclodextrin Complexes Revealed by NMR Spectroscopy in Salt Water

Multitopic supramolecular guests with finely tuned affinities toward widely explored cucurbit[n]urils (CBs) and cyclodextrins (CDs) have been recently designed and tested as functional components of advanced supramolecular systems. We employed various spa

Synthesis of 1,4-Disubstituted 1 H -1,2,3-Triazoles from 4-(1-Adamantyl)benzyl Azide through a 1,3-Dipolar Cycloaddition Reaction

A series of new 1,4-disubstituted 1 H -1,2,3-triazole derivatives were synthesized by an efficient copper-catalyzed 1,3-dipolar cycloaddition reaction of 4-(1-adamantyl)benzyl azide with several terminal alkynes. The copper catalyst was used to provide 1,