6543-57-3

Basic information

• Product Name: 13,14-(1,3-Butadiene-1,4-diyl)-[9,10-(1,3-butadiene-1,4-diyl)-[5,6-(1,3-butadiene-1,4-diyl)-[1,2-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone]]]
• Synonyms: 1,2-(1,3-Butadiene-1,4-diyl)-5,6-(1,3-butadiene-1,4-diyl)-9,10-(1,3-butadiene-1,4-diyl)-13,14-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone;13,14-(1,3-Butadiene-1,4-diyl)-[9,10-(1,3-butadiene-1,4-diyl)-[5,6-(1,3-butadiene-1,4-diyl)-[1,2-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone]]];2-[[2-[[2-[(2-Hydroxybenzoyl)oxy]benzoyl]oxy]benzoyl]oxy]benzoic acid lactone;6H,12H,18H,24H-5,11,17,23-Tetraoxatetrabenzo[a,e,i,m]cyclohexadecene-6,12,18,24-tetrone;6H,12H,18H,24H-Tetrabenzo[b,f,j,n][1,5,9,13]tetraoxacyclohexadecin-6,12,18,24-tetrone;Tetrasalicylide
• CAS NO: 6543-57-3
• Molecular Formula: C₂₈H₁₆O₈
• Molecular Weight: 480.42
• Mol File: 6543-57-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 700.6°C at 760 mmHg
• Flash Point: 300.3°C
• Appearance: /
• Density: 1.36g/cm³
• Vapor Pressure: 1.78E-19mmHg at 25°C
• Refractive Index: 1.618
• CAS DataBase Reference: 13,14-(1,3-Butadiene-1,4-diyl)-[9,10-(1,3-butadiene-1,4-diyl)-[5,6-(1,3-butadiene-1,4-diyl)-[1,2-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone]]](CAS DataBase Reference)
• NIST Chemistry Reference: 13,14-(1,3-Butadiene-1,4-diyl)-[9,10-(1,3-butadiene-1,4-diyl)-[5,6-(1,3-butadiene-1,4-diyl)-[1,2-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone]]](6543-57-3)
• EPA Substance Registry System: 13,14-(1,3-Butadiene-1,4-diyl)-[9,10-(1,3-butadiene-1,4-diyl)-[5,6-(1,3-butadiene-1,4-diyl)-[1,2-(1,3-butadiene-1,4-diyl)-4,8,12,16-tetraoxacyclohexadecane-1,5,9,13-tetraene-3,7,11,15-tetraone]]](6543-57-3)

Safety Data

• Hazardous Substances Data: 6543-57-3(Hazardous Substances Data)

Usage

Molecular structure

A complex organic compound with a long and intricate structure.

Explanation

The compound consists of multiple repeated units of 1,3-butadiene, connected in a specific arrangement.

Explanation

The presence of multiple 1,3-butadiene units in the compound contributes to its reactivity and flammability.

Explanation

The presence of this ring structure indicates a high degree of cyclic organization within the compound.

Explanation

The complex structure and multiple functional groups suggest that the compound may be a polymer or a macrocycle, which could have various applications in these fields.

Explanation

The multiple butadiene units in the compound make it a suitable candidate for polymerization or as a starting material for synthesizing other organic compounds.

1,3-Butadiene units

Highly reactive and flammable.

Tetraoxacyclohexadecane

A 16-membered oxygen-containing ring within the molecule.

Polymer or macrocycle

Potential applications in materials science or pharmaceuticals.

Polymerization potential

Possible use in polymerization processes or as a precursor for organic synthesis.

InChI:InChI=1/C28H16O8/c29-25-17-9-1-5-13-21(17)33-26(30)19-11-3-7-15-23(19)35-28(32)20-12-4-8-16-24(20)36-27(31)18-10-2-6-14-22(18)34-25/h1-16H

Upstream product

• 69-72-7 salicylic acid 

Downstream Products

• 552-94-3 2-hydroxy-benzoic acid, 2-carboxyphenyl ester 

Relevant articles and documents

Inclusion and gelation properties of novel tetra- and hexasalicylide derivatives

(Chemical Equation Presented) Some novel tetra- and hexasalicylide derivatives were synthesized. The tetrasalicylides having a 5-substituted halogen atom on the aromatic ring form organogels with several kinds of organic solvents, whereas the parent compound does not. In contrast, hexasalicylides form stable inclusion crystals with several organic guest molecules.