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Usage

Uses

Used in Organic Chemistry:
1,3-BIS(4-METHYLPHENYL)ADAMANTANE is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Development:
Due to its unique and rigid structure, 1,3-BIS(4-METHYLPHENYL)ADAMANTANE is used as a structural component in the development of new pharmaceuticals, potentially enhancing the properties and effectiveness of drug candidates.
Used in Advanced Materials:
1,3-BIS(4-METHYLPHENYL)ADAMANTANE is used as a component in the creation of advanced materials, leveraging its structural properties to improve material performance and characteristics.
Used in Nanotechnology:
The rigid and unique structure of 1,3-BIS(4-METHYLPHENYL)ADAMANTANE makes it a candidate for use in nanotechnology applications, where its properties can be exploited to create novel nanoscale devices and systems.

InChI:InChI=1S/C24H28/c1-17-3-7-21(8-4-17)23-12-19-11-20(13-23)15-24(14-19,16-23)22-9-5-18(2)6-10-22/h3-10,19-20H,11-16H2,1-2H3

Upstream product

• 281-23-2 adamantane 
• 108-88-3 toluene 
• 53488-28-1 dinitrate of 1,3-adamantanediol 
• 6465-33-4 3-methyl-2-oxa-1-adamantantanol 

Relevant academic research and scientific papers

Easy synthesis of 7-alkylbicyclo[3.3.1]non-6-en-3-ones by silica gelpromoted fragmentation of 3-alkyl-2-oxaadamant-1-yl mesylates

A synthesis of 7-alkylbicyclo[3.3.1]non-6-en-3-ones 4b-f and 4j,k by reaction of the corresponding 3-alkyl-2-oxaadamant-1-yl mesylates 3 with silica gel in methylene chloride at room temperature, is described. The method failed to give enones 4a,g and the

Direct Clay-Catalyzed Friedel-Crafts Arylation and Chlorination of the Hydrocarbon Adamantane

Multiple chlorinations and arylations at the tertiary positions of adamantane are promoted by FeCl3-doped K10 montmorillonite in CCl4 or in aromatic solvents.The process, remarkably easy implement, can be tailored to selective formation of monosubstituted 1-adamantyl derivatives or 1,3-disubstituted adamantanes.The process achieves alkylation at the meta- and para-positions of toluene leading to a purely statistical distribution and displays no substrate specificity in competition experiments between toluene and benzene.

REACTIONS OF ADAMANTYL NITRATES WITH AROMATIC COMPOUNDS.

It has been shown to be possible to use adamantyl nitrates in the synthesis of mono- and diaryladamantanes.The effects of substituents and the acidity of the medium on the yields of reaction products have been studied.