13630-39-2

Basic information

• Product Name: 1,1,1-triphenylpentane
• Synonyms: 1,1,1-triphenylpentane
• CAS NO: 13630-39-2
• Molecular Weight: 300.444
• Mol File: 13630-39-2.mol

Chemical Properties

• CAS DataBase Reference: 1,1,1-triphenylpentane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,1-triphenylpentane(13630-39-2)
• EPA Substance Registry System: 1,1,1-triphenylpentane(13630-39-2)

Safety Data

• Hazardous Substances Data: 13630-39-2(Hazardous Substances Data)

Upstream product

• 109-72-8 n-butyllithium 
• 76-83-5 trityl chloride 
• 109-65-9 1-bromo-butane 
• 733-89-1 triphenylmethane cesium salt 
• 33884-98-9 5-Chlor-1,1,1-triphenylpentan 
• 13630-38-1 1,1,1-Triphenyl-2,4-pentadien 
• 519-73-3 triphenylmethane 
• 13630-30-3 1-Chlor-5,5,5-triphenyl-penten-⁽²⁾ 

Downstream Products

• 1246560-72-4 1,1,1-tris(4-nitrophenyl)pentane 
• 102541-84-4 1,1,1-tricyclohexyl-pentane 
• 112685-73-1 1,1-dicyclohexyl-1-phenyl-pentane 

Relevant articles and documents

Combining metallasupramolecular chemistry with dynamic covalent chemistry: Synthesis of large molecular cages

(Figure Presented) Ru-built cube: By combining metallasupramolecular chemistry with dynamic covalent chemistry, complex nanostructures can be formed. Large cages are synthesized by reaction of trinuclear metallamacrocycles containing pendant aldehyde groups (see picture; Ru blue, aldehyde linkers green) with triamines (red).

REACTIVITY OF CARBANIONS. VIII. REACTION OF ALKALI SALTS OF TRIPHENYLMETHANE WITH ALKYL HALIDES

The kinetics of the alkylation of the lithium, sodium, and cesium salts of triphenylmethane by alkyl chlorides and butyl bromide in dimethoxyethane and tetrahydrofuran at 25 deg.C were investigated.It was established that the rate constant for the reaction of the free triphenylmethyl anion is almost three orders of magnitude greater than the rate constant for the reaction of the intimate cesium ion pairs and two to three times greater than the rate constant for the reaction of the solvent-separated lithium ion pairs.The reactivity of normal alkanes in reaction both with the free anion and with the ion pairs increases in the order C4H9Cl C3H7Cl C2H5Cl CH3Cl.