CAS 20115-81-5

2,2'-[ethane-1,2-diylbis(oxy)]diphenol

Description:

2,2'-[Ethane-1,2-diylbis(oxy)]diphenol, commonly known as bisphenol F (BPF), is an organic compound characterized by its structure, which features two phenolic groups connected by an ethane-1,2-diyl (ethylene glycol) bridge. This compound is a colorless solid at room temperature and is soluble in organic solvents but has limited solubility in water. BPF exhibits properties typical of phenolic compounds, including the ability to form hydrogen bonds, which contributes to its reactivity and potential applications in polymer chemistry. It is primarily used as a monomer in the production of epoxy resins and other thermosetting plastics, offering good thermal stability and mechanical strength. Additionally, BPF has been studied for its endocrine-disrupting potential, raising concerns regarding its safety in consumer products. Its chemical stability and reactivity make it a valuable compound in various industrial applications, while ongoing research continues to evaluate its environmental impact and health effects.

Formula: C₁₄H₁₄O₄

InChI: InChI=1/C14H14O4/c15-11-5-1-3-7-13(11)17-9-10-18-14-8-4-2-6-12(14)16/h1-8,15-16H,9-10H2

SMILES: c1ccc(c(c1)O)OCCOc1ccccc1O

Synonyms:

• Phenol, 2,2'-[1,2-Ethanediylbis(Oxy)]Bis-
• Phenol, 2-{2-(2-hydroxyphenoxy)ethoxy}
• 2,2'-[Ethane-1,2-diylbis(oxy)]diphenol

2,2'-Ethylenedioxydiphenol

CAS: 20115-81-5

Formula: C₁₄H₁₄O₄

Purity: >98.0%(GC)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 246.26

Ref: 3B-E0557

1,2-Bis(2-hydroxyphenoxy)ethane

CAS: 20115-81-5

Formula: C₁₄H₁₄O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 246.2586

Ref: IN-DA002D8R

2,2′-(Ethane-1,2-diylbis(oxy))diphenol

CAS: 20115-81-5

Purity: ≥98%

Molecular weight: 246.2619934

Ref: 10-F725158

2,2'-Ethylenedioxydiphenol

CAS: 20115-81-5

2,2'-Ethylenedioxydiphenol is a cation that is used as an intermediate in the synthesis of glycols, esters, and polyethylene glycols. It can also be used to catalyze reactions involving aliphatic compounds and ethers. 2,2'-Ethylenedioxydiphenol has been shown to react with dichlorides to form ethyl esters. This reaction proceeds via two pathways: one involving macrocyclic intermediates and the other involving aliphatic intermediates. The constants of these two pathways are different.

Formula: C₁₄H₁₄O₄

Purity: Min. 95%

Molecular weight: 246.26 g/mol

Ref: 3D-VAA11581