287924-56-5

Basic information

• Product Name: 5-BROMO-7-(5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE
• Synonyms: 5-BROMO-7-(5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE;7,7'-dibromo-2,2',3,3'-tetrahydro-5,5'-bithieno[3,4-b][1,4]dioxine;5,5'-Bithieno[3,4-b]-1,4-dioxin,7,7'-dibromo-2,2',3,3'-tetrahydro-;5,5'-dibromo-2,2'-bis[(3,4-ethylenedioxy)thiophene]
• CAS NO: 287924-56-5
• Molecular Formula: C12H8Br2O4S2
• Molecular Weight: 440.13
• Mol File: 287924-56-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 483.7±45.0 °C(Predicted)
• Appearance: /
• Density: 1.965±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 5-BROMO-7-(5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-7-(5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE(287924-56-5)
• EPA Substance Registry System: 5-BROMO-7-(5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE(287924-56-5)

Safety Data

• Hazardous Substances Data: 287924-56-5(Hazardous Substances Data)

Usage

General Description

5-Bromo-7-(5-bromo-2,3-dihydrothieno[3,4-b][1,4]dioxin-7-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxine is a compound with a complex chemical structure, consisting of two fused thiophene rings and dioxin groups. The presence of bromine atoms at positions 5 and 7 on the molecule further adds to its unique properties. This chemical may have potential applications in pharmaceutical research, as the presence of heterocyclic rings and bromine atoms can influence its reactivity and biological activity. Further studies are needed to fully understand the potential uses and effects of this compound.

Upstream product

• 195602-17-6 2,2'-bis(3,4-ethylenedioxythiophene) 

Downstream Products

• 1415917-14-4 C₃₂H₃₄O₈S₂ 

Relevant articles and documents

Stable and soluble oligo(3,4-ethylenedioxythiophene)s end-capped with alkyl chains

The synthesis of a new series of stable and soluble EDOT oligomers end-capped with n-hexyl groups is described. Optical and electrochemical results indicate that the synergy between the direct electron-releasing effects of the ethylenedioxy groups and the self-rigidification resulting from intramolecular interactions controls to a large extent the HOMO-LUMO gap.