19496-84-5

Basic information

• Product Name: 1-Bromomethyl-o-carborane
• Synonyms: 1-Bromomethyl-o-carborane;1,2-Dicarbadodecaborane(12), 1-(bromomethyl)-
• CAS NO: 19496-84-5
• Molecular Formula: C₃H₁₃B₁₀Br
• Molecular Weight: 237.15
• Mol File: 19496-84-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Bromomethyl-o-carborane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromomethyl-o-carborane(19496-84-5)
• EPA Substance Registry System: 1-Bromomethyl-o-carborane(19496-84-5)

Safety Data

• Hazardous Substances Data: 19496-84-5(Hazardous Substances Data)

Usage

General Description

1-Bromomethyl-o-carborane is a chemical compound with the molecular formula C2HB10Br, consisting of a carborane cage with a bromomethyl group attached to one of the carbon atoms. It is a halogenated derivative of o-carborane, which is a type of boron cluster compound. This chemical is used in various applications, including as a reagent in organic synthesis and as a building block for the preparation of other functionalized carboranes. It is known for its high thermal and chemical stability, as well as its ability to form strong covalent bonds, making it a valuable tool in the field of organometallic chemistry.

Downstream Products

• 16872-10-9 1-methyl-o-carborane 
• 20740-05-0 1-(n-hexyl)-1,2-dicarba-closo-dodecaborane 
• 1299472-30-2 1-[(4-(2-methoxyphenyl)piperazin-1-yl)methyl]-1,2-dicarba-closo-dodecaborane 
• 219864-16-1 1,2-dicarba-closo-dodecaboran-1-yl-methyl-MgCl 
• 20199-64-8 C-carboranylmethylmagnesium bromide 
• 17805-87-7 1-CH₃-2-MgBr-1.2-C₂B₁₀H₁₀ 
• 123462-81-7 9-(o-carboran-1-ylmethyl)-o-carborane 

Related news

Nickel-catalyzed cross-coupling of sterically hindered 1-Bromomethyl-o-carborane (cas 19496-84-5) with alkyl and aryl Grignard reagents08/21/2019

A convenient and efficient Ni-catalyzed reaction has been developed for synthesis of mono-substituted o-carboranes, involving cross-coupling of readily available and sterically hindered 1-bromomethyl-o-carborane with various alkyl and aryl Grignard reagents under mild conditions, and the corresp...detailed