82645-24-7

Basic information

• Product Name: 1,2-Bis[2-(2-formylphenoxy)ethoxy]ethane
• Synonyms: 1,2-Bis[2-(2-formylphenoxy)ethoxy]ethane;1,2-bis[2-(2-formylphenoxy) ethoxy]ethan
• CAS NO: 82645-24-7
• Molecular Formula: C₁₈H₁₈O₅
• Molecular Weight: 358.38508
• Mol File: 82645-24-7.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Bis[2-(2-formylphenoxy)ethoxy]ethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Bis[2-(2-formylphenoxy)ethoxy]ethane(82645-24-7)
• EPA Substance Registry System: 1,2-Bis[2-(2-formylphenoxy)ethoxy]ethane(82645-24-7)

Safety Data

• Hazardous Substances Data: 82645-24-7(Hazardous Substances Data)

Usage

Type of compound

bisphenol

Usage

production of epoxy resins, cross-linking agent in polymer chemistry, building block in synthesis of organic compounds and materials

Structure

two ethylene glycol side chains connected to an ethane backbone, each containing a formylphenoxy group

Hazardous nature

potentially hazardous chemical, should be handled with care due to potential health and environmental effects

Upstream product

• 90-02-8 salicylaldehyde 
• 90-01-7 salicylic alcohol 
• 7460-82-4 diethylene glycol ditosylate 
• 5414-19-7 1,1'-oxybis(2-bromo-ethane) 
• 89-95-2 2-methyl-benzyl alcohol 
• 3116-83-4 sodium salicylate 
• 111-44-4 3-oxa-1,5-dichloropentane 

Relevant articles and documents

Spectroscopic and electrochemical studies of transition metal complexes with N,N′-bis(2-aminothiophenol)-1,7-bis(2-formylphenyl)-1,4,7- trioxaheptane and structure effects on extractability of ligand towards some divalent cations

La(III), Cu(II), Ni(II), and Zn(II) metal complexes with a novel quadridentate Schiff base derived from 1,7-bis(2-formylphenyl)-1,4,7- trioxaheptane and 2-aminothiophenol were synthesized and characterized by microanalytical data, elemental analysis, magn

DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA

Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are dimeric inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

Synthesis and characterization of novel biological tetracoumarin derivatives bearing ether moieties

A series of novel tetracoumarin derivatives (3a-f) were prepared using the reaction of ether functionalized dibenzaldehyde with 4-hydroxycoumarin in the presence of sodium acetate. The structure of compounds was validated by IR, NMR, and CHN analyzes. Antimicrobial (antibacterial and antifungal) activity was studied on the basis of the minimum bactericidal concentration, minimum inhibitory concentration and inhibitory zone diameter. Favorable biological activity was found in compound 3f.

Exploitation of Intramolecular Glaser-Eglinton-Hay Macrocyclization for the Synthesis of New Classes of Optically Active Aza-Oxo-Thia Polyether Macrocycles from Amino Alcohol Building Blocks

We report an intramolecular Glaser-Eglinton-Hay coupling as an unprecedented route for assembling optically active aza-oxo polyether macrocycles containing a 1,3-diyne unit from enantiopure amino alcohol building blocks and suitable linkers. Furthermore, the conversion of the 1,3-diyne unit of the aza-oxo polyether macrocycles into a thiophene ring led to the assembly of new classes of optically active aza-oxa-thia (heterotopic) polyether macrocycle analogues of classical 18-C-6 and 18-C-5 systems.