40775-32-4

Basic information

• Product Name: Benzene, 1,4-diheptyl-
• CAS NO: 40775-32-4
• Molecular Formula: C20H34
• Molecular Weight: 274.49
• Mol File: 40775-32-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,4-diheptyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,4-diheptyl-(40775-32-4)
• EPA Substance Registry System: Benzene, 1,4-diheptyl-(40775-32-4)

Safety Data

• Hazardous Substances Data: 40775-32-4(Hazardous Substances Data)

Upstream product

• 629-04-9 1-Bromoheptane 
• 106-37-6 1.4-dibromobenzene 
• 106-46-7 para-dichlorobenzene 
• 13125-66-1 n-heptylmagnesium bromide 
• 72245-81-9 9-heptyl-9-borabicyclo<3,3,1>nonane 
• 7608-06-2 n-heptylzinc bromide 
• 1078-71-3 heptylbenzene 
• 1671-75-6 Heptanophenone 
• 165727-35-5 1,4-di(1'-hydroxyheptyl)-benzene 
• 623-27-8 terephthalaldehyde, 
• 111-25-1 1-bromo-hexane 
• 165727-41-3 1,4-Bis-((E)-hept-1-enyl)-benzene 
• 85196-60-7 1,1'-(1,4-phenylene)bis-1-heptanone 
• 89583-95-9 Hexylmagnesiumiodid 

Downstream Products

• 19859-22-4 2,5-Diheptyl-benzolsulfanilid 
• 33104-78-8 2,5-Di-n-heptylstyrol 
• 32937-64-7 2,5-Di-n-heptylphenyl-methylcarbinol 
• 187326-87-0 1,4-Dibromo-2,5-diheptylbenzene 
• 96375-61-0 1,4-Diheptyl-benzol-2-sulfonsaeure 
• 102464-94-8 1,4-Diheptyl-cyclohexan 
• 141102-64-9 C₂₆H₄₈S₂⁽²⁺⁾*2Cl^(1-) 
• 141123-78-6 2,5-bis(chloromethyl)-1,4-diheptylbenzene 
• 259886-75-4 2,5-Diheptylbenzeneboronic acid 
• 259886-74-3 1-Bromo-2,5-diheptylbenzene 
• 33104-72-2 2,5-Di-n-heptylacetophenon 

Relevant articles and documents

Preparation of Poly(2,5-diheptyl-1,4-phenylenevinylene) by Sulfonium Salt Pyrolysis

Poly(2,5-diheptyl-1,4-phenylenevinylene) (1) was prepared by the sulfonium salt pyrolysis procedure.Tough films of 1 were obtained by pyrolysis of its sulfonium salt precursor film.Due to flexible side chains, 1 was soluble in organic solvents such as chloroform.The molecular weights were Mn=3.8-4.7*104 and Mw=1.4-1.8*105.The ratio of trans to cis olefinic units was found to be 93:7 from the 1H NMR spectrum.Two arylmethylene peaks suggested that there were two kinds of stereochemically different methylene groups.Although the peak energy in the absorption spectra was almost identical to those of poly(1,4-phenylenevinylene) (PPV), the electrical conductivity of 1 was much lower than that of PPV.

SYNTHESIS AND SPECTROSCOPY OF 1,4-DIALKYLBENZENES

Five linear 1,3-dialkylbenzenes namely, dibutyl-, dipentyl-, dihexyl-, diheptyl- and dioctylbenzenes were prepared in good yield via two simple catalytic routes under very mild conditions and affording insignificant side products, The starting feed, 1,4-d