104388-17-2

Basic information

• Product Name: Benzene, (1,2-dimethyl-1-propylbutyl)-
• CAS NO: 104388-17-2
• Molecular Formula: C15H24
• Molecular Weight: 204.356
• Mol File: 104388-17-2.mol

Chemical Properties

• CAS DataBase Reference: Benzene, (1,2-dimethyl-1-propylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1,2-dimethyl-1-propylbutyl)-(104388-17-2)
• EPA Substance Registry System: Benzene, (1,2-dimethyl-1-propylbutyl)-(104388-17-2)

Safety Data

• Hazardous Substances Data: 104388-17-2(Hazardous Substances Data)

Upstream product

• 105824-39-3 (1,1-Bis-methylselanyl-butyl)-benzene 
• 98-86-2 acetophenone 
• 495-40-9 propiophenone 
• 100-52-7 benzaldehyde 
• 94417-53-5 (1-phenylethane-1,1-diyl)bis(methylselane) 
• 94417-52-4 (Bis-methylselanyl-methyl)-benzene 
• 4383-18-0 2-phenyl-pentan-2-ol 
• 104388-11-6 (1-Methyl-1-methylselanyl-butyl)-benzene 
• 78-76-2 s-butyl bromide 

Relevant articles and documents

METALLATION OF BENZYL SELENIDES AND OF α-ARYL SELENOACETALS. SCOPE AND LIMITATIONS.

α-Metallo benzylselenides and α-metallo selenoacetals derived from aromatic aldehydes have been conveniently prepared by metallation of the corresponding carbon acids.KDA in THF proved among the various basic systems tested, the most efficient.

A NOVEL METHOD FOR THE GEMINAL DIALKYLATION OF THE CARBONYL GROUP OF AROMATIC ALDEHYDES AND KETONES

The title transformation is efficiently achieved by using the selenium methodology which involves the sequential reductive alkylation of arylselenoacetals and of benzylselenides.

Novel Synthetic Route to Aryl Alkanes from Aromatic Aldehydes and Ketones. Novel Geminal Dialkylation of the Carbonyl Group of Aromatic Aldehydes and Ketones

Benzyl-lithiums, readily available from benzyl methyl selenides and alkyl-lithiums, are efficiently alkylated; this reaction allows the geminal dialkylation of the carbonyl groups of aromatic aldehydes and ketones and the geminal aryl-alkylation of aliphatic analogues.