65128-45-2

Basic information

• Product Name: 1,4-DI(HEPTYLOXY)BENZENE
• Synonyms: 1,4-DI(HEPTYLOXY)BENZENE;1,4-bis(heptyloxy)benzene
• CAS NO: 65128-45-2
• Molecular Formula: C₂₀H₃₄O₂
• Molecular Weight: 306.48
• Mol File: 65128-45-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-DI(HEPTYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DI(HEPTYLOXY)BENZENE(65128-45-2)
• EPA Substance Registry System: 1,4-DI(HEPTYLOXY)BENZENE(65128-45-2)

Safety Data

• Hazardous Substances Data: 65128-45-2(Hazardous Substances Data)

Usage

Uses

1,4-Bis(heptyloxy)benzene is a useful synthesis intermediate.

Upstream product

• 629-04-9 1-Bromoheptane 
• 7664-46-2 disodium salt of hydroquinone 
• 123-31-9 hydroquinone 
• 4282-40-0 1-Iodoheptane 

Downstream Products

• 77855-11-9 1,4-Diheptyloxy-2,3-dinitrobenzene 
• 81259-73-6 1,4-Bis-heptyloxy-2-nitro-benzene 
• 149762-42-5 1,4-diiodo-2,5-diheptyloxybenzene 
• 206762-48-3 2,5-di-(n-heptyloxy)terephthaldialdehyde 
• 902459-64-7 4-(4-methoxy-α-cyanostyryl)-2,5-di-(n-heptyloxy)benzaldehyde 
• 190130-75-7 2,5-Bis-heptyloxy-4-iodo-benzaldehyde 
• 81259-75-8 4-Heptyloxy-2-nitro-phenol 
• 79887-27-7 4-Butyl-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-29-9 4-Heptyl-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-31-3 4-Hexyloxy-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-33-5 (E)-3-(4-Heptyl-phenyl)-acrylic acid 4-heptyloxy-2-nitro-phenyl ester 
• 77855-25-5 Bis-(3,6-bis-heptyloxy-2-nitro-phenyl)-diazene 
• 171569-05-4 1,4-bis(trimethylstannyl)-2,5-bis(heptyloxy)benzene 

Relevant articles and documents

Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs

Complexation of achiral pillar[5]arenes with chiral amines induced strong circular dichroism (CD) signals. The CD responses differed drastically depending on the nature of the amino acid guest, and they significantly varied and part of them even inverted, upon increasing the length of the alkyl chains of the pillar[5]arenes guests. Accordingly, this tactic allowed for the unprecedented simultaneous enantiomeric and structural differentiation of α-amino esters with homologous molecular hosts.

Aryl trihydroxyborate salts: Thermally unstable species with unusual gelation abilities

A series of aryl trihydroxyborate salts were synthesized and found to form gels in benzene. The compounds were thermally unstable and readily underwent protodeboronation in solution and the solid state. Gelation could be induced without decomposition via sonication. Subsequent characterization studies revealed an unusual dependence of gel properties on alkyl chain length.