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

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 
• 4282-40-0 1-Iodoheptane 
• 123-31-9 hydroquinone 

Downstream Products

• 1334177-72-8 (2,5-bis(heptyloxy)phenyl)boronic acid 
• 1334177-76-2 (4-bromo-2,5-bis(heptyloxy)phenyl)boronic acid 
• 1334177-65-9 2-bromo-1,4-bis(heptyloxy)benzene 
• 137436-29-4 1,4-dibromo-2,5-bis(heptyloxy)benzene 
• 171569-05-4 1,4-bis(trimethylstannyl)-2,5-bis(heptyloxy)benzene 
• 77855-25-5 Bis-(3,6-bis-heptyloxy-2-nitro-phenyl)-diazene 
• 79887-33-5 (E)-3-(4-Heptyl-phenyl)-acrylic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-31-3 4-Hexyloxy-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-29-9 4-Heptyl-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 79887-27-7 4-Butyl-benzoic acid 4-heptyloxy-2-nitro-phenyl ester 
• 81259-75-8 4-Heptyloxy-2-nitro-phenol 
• 190130-75-7 2,5-Bis-heptyloxy-4-iodo-benzaldehyde 

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.

Solvent-free synthesis of pillar[6]arenes

An efficient solvent-free procedure for the synthesis of pillar[6]arenes has been developed. The procedure involves the solid-state condensation of finely milled 1,4-dialkoxybenzene and paraformaldehyde by grinding in the presence of a catalytic amount of H2SO4. The use of organic solvents for the extraction of products has also been avoided. Operational simplicity, compatibility with various 1,4-dialkoxybenzenes, non-chromatographic purification technique, high yields and mild reaction conditions are the notable advantages of this procedure. A large scale reaction demonstrated the practical applicability of this methodology.

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.

Synthesis and characterization of photorefractive polymers containing transition metal complexes as photosensitizer

This paper reports detailed synthesis and characterization of a hybridized polymer system which combines the ionic transition metal complexes and a conjugated polymer backbone bearing NLO chromophores to manifest a large photorefractive (PR) effect. In th