CAS 19190-91-1

Acenaphthylene, 5,6-dibromo-1,2-dihydro-

Description:

Acenaphthylene, 5,6-dibromo-1,2-dihydro- is a brominated derivative of acenaphthylene, a polycyclic aromatic hydrocarbon. This compound features a fused bicyclic structure, which contributes to its unique chemical properties. The presence of bromine atoms at the 5 and 6 positions enhances its reactivity, making it useful in various chemical syntheses and applications. Typically, such brominated compounds exhibit increased polarity and can participate in electrophilic substitution reactions. The dihydro form indicates that it has undergone partial hydrogenation, which can affect its stability and reactivity compared to its fully aromatic counterparts. Acenaphthylene derivatives are often studied for their potential applications in organic electronics, materials science, and as intermediates in organic synthesis. Safety data should be consulted, as brominated compounds can pose environmental and health risks due to their potential toxicity and persistence. Overall, the characteristics of this compound make it a subject of interest in both academic research and industrial applications.

Formula: C₁₂H₈Br₂

InChI: InChI=1/C12H8Br2/c13-9-5-3-7-1-2-8-4-6-10(14)12(9)11(7)8/h3-6H,1-2H2

SMILES: C1Cc2ccc(c3c(ccc1c23)Br)Br

Synonyms:

• 5,6-Dibromo-1,2-dihydroacenaphthylene
• acenaphthylene, 5,6-dibromo-1,2-dihydro-

5,6-Dibromo-1,2-dihydroacenaphthylene

CAS: 19190-91-1

Formula: C₁₂H₈Br₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 311.9999

Ref: IN-DA002FJY

5,6-Dibromo-1,2-dihydroacenaphthylene

CAS: 19190-91-1

5,6-Dibromo-1,2-dihydroacenaphthylene

Purity: 99%

Molecular weight: 312g/mol

Ref: 54-OR1028503

5,6-Dibromo-1,2-dihydroacenaphthylene

CAS: 19190-91-1

Purity: 95.0%

Color and Shape: Liquid, No data available.

Molecular weight: 312.0039978027344

Ref: 10-F498067

5,6-Dibromoacenaphthene

CAS: 19190-91-1

5,6-Dibromoacenaphthene is a naphthalene derivative that has been used as a starting material for the synthesis of organometallic compounds. It can be synthesized by reacting butyllithium with 2-bromoacetophenone in presence of an organic acid such as ammonium salt or boronic acid. The reaction product can then be treated with allyl bromide to produce 5,6-dibromoacenaphthene. This compound has been used as a precursor for the production of diphenols and phosphines. 5,6-Dibromoacenaphthene interacts with strong bases such as alkali metals and amines.

Formula: C₁₂H₈Br₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 312 g/mol

Ref: 3D-FD67422