17976-92-0

Usage

Chemical family

Acenaphthene derivatives

Structure

A naphthalene group with two hydroxyl groups attached to adjacent carbon atoms

Molecular weight

190.21 g/mol

Appearance

Unknown, as it is primarily used for research purposes

Solubility

Unknown, but likely soluble in organic solvents due to its hydrocarbon backbone

Melting point

Unknown, as it is primarily used for research purposes

Boiling point

Unknown, as it is primarily used for research purposes

Density

Unknown, as it is primarily used for research purposes

Stability

Unknown, but may be sensitive to oxidation or other reactions due to the presence of hydroxyl groups

Reactivity

Likely to undergo reactions typical of aromatic compounds, such as electrophilic substitution, and may also participate in reactions involving the hydroxyl groups, such as esterification or condensation

Uses

Primarily used for research purposes, with potential applications in organic synthesis and as a building block for the development of new compounds with potential pharmaceutical or industrial applications

Safety

Further research is needed to fully understand the potential hazards and safety precautions associated with 1,2-dihydroacenaphthylene-1,2-diol

Environmental impact

Further research is needed to fully understand the potential environmental impact of 1,2-dihydroacenaphthylene-1,2-diol

Synthesis

The synthesis of 1,2-dihydroacenaphthylene-1,2-diol is not well-documented, but it is likely synthesized through chemical reactions involving acenaphthylene or related compounds

Further research

The properties and potential applications of 1,2-dihydroacenaphthylene-1,2-diol are still being studied, and further research is needed to fully understand its potential uses and properties.

Upstream product

• 82-86-0 acenaphthene quinone 
• 1663-45-2 1,2-bis-(diphenylphosphino)ethane 
• 14209-08-6 1,2-dibromoacenaphthene 
• 7732-18-5 water 
• 5448-26-0 1,2-dichloro-acenaphthene 
• 38023-74-4 Acenaphthylene glycol monoacetate 

Downstream Products

• 518-05-8 Naphthalene-1,8-dicarboxylic acid 
• 2235-15-6 1(2H)-acenaphthylenone 
• 17216-14-7 naphthalene-1,8-dicarbaldehyde 
• 13362-59-9 9-methyl-acenaphtho[1,2-b]quinoxaline 
• 16269-27-5 2-bromoacenaphthylen-1(2H)-one 

Relevant academic research and scientific papers

On the redox reaction of 1,2-bis(diphenylphosphino) alkanes toward o -, and p-quinones

The reaction of 1,2-bis(diphenylphosphino)ethane with substituted o-benzo-quinones afforded new bis(6-hydroxycyclohexa-2,4-dienone) derivatives. Treatment of the same reagent with o-naphthoquinone, phenanthrenequinone, and acenaphthenequinone gave the res

An original on-column oxidative cleavage of vicinal diols using alumina/potassium periodate: Application to sequential oxidation/Horner-Emmons reactions

An unprecedented simple on-column solvent-free oxidative cleavage of vicinal diols in the solid phase using alumina/potassium metaperiodate is described herein. It permits preparation of the corresponding carbonyl compounds with high purity and good to excellent yields requiring only short reaction times. This methodology is then employed in on-column sequential oxidation/Horner-Emmons reactions for the preparation of selected stilbenes in good yields where both reaction and purification are integrated in a single unit or occur simultaneously permitting the rapid and easy preparation of small samples of pure stilbenes. The on-column oxidative cleavage of vicinal diols using alumina/potassium periodate is investigated. This approach is then applied to sequential oxidation/Horner-Emmons reactions for the simultaneous preparation and purification of stilbenes in good yields and requiring short reaction times.

Preparation of chiral trans-5-substituted-acenaphthene-1,2-diols by baker's yeast-mediated reduction of 5-substituted-acenaphthylene-1,2-diones

A series of trans-5-substituted-acenaphthene-1,2-diols were obtained in 21-72% yield with 97-100% ee by baker's yeast-mediated reduction of the corresponding acenaphthylene-1,2-diones, in the presence of DMSO as a co-solvent and under vigorous agitation.

Modofied Borohydride Agents, (1,4-Diazabicyclooctane)(tetrahydroboronato)zinc Complex . A New Ligand Metal Borohydride as a Stable, Efficient, and Versatile Reducing Agent

(1,4-Diazabicyclooctane)(tetrahydroborato)zinc complex is a stable compound which has been used for the selective reduction of aldehydes, ketones, α,β-unsaturated carbonyl compounds, α-diketones, acyloins and acyl chlorides to their alcohols and aldehydes in THF or CH2Cl2/hexane at room temperature or under reflux conditions.