52376-16-6

Usage

Uses

1. Used in Chemical Synthesis:
1,4-Diacetoxy-2-bromobenzene 97 is used as a key intermediate in the synthesis of various organic compounds, such as bromohydroquinone and (Sp,S)-1-(2,5-diacetoxyphenyl)-2-(p-tolylsulfinyl)ferrocene. Its unique structure allows for further chemical reactions and modifications, making it a valuable building block in the development of new molecules with specific properties and applications.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Diacetoxy-2-bromobenzene 97 may be utilized as a starting material for the development of new drugs or drug candidates. Its chemical structure can be further modified to create compounds with potential therapeutic effects, targeting various diseases and medical conditions.
3. Used in Material Science:
1,4-Diacetoxy-2-bromobenzene 97 can also be employed in the field of material science, where its unique chemical properties may be harnessed to develop new materials with specific characteristics. These materials could have applications in various industries, such as electronics, automotive, or aerospace.
4. Used in Research and Development:
As a versatile organic compound, 1,4-Diacetoxy-2-bromobenzene 97 is also used in research and development laboratories. Scientists and researchers can explore its chemical properties and potential applications, leading to the discovery of new compounds and technologies that can benefit various industries.

InChI:InChI=1/C10H9BrO4/c1-6(12)14-8-3-4-10(9(11)5-8)15-7(2)13/h3-5H,1-2H3

Upstream product

• 583-69-7 2-bromobenzene-1,4-diol 
• 108-24-7 acetic anhydride 
• 506-96-7 Acetyl bromide 
• 106-51-4 p-benzoquinone 
• 64-19-7 acetic acid 
• 123-31-9 hydroquinone 

Downstream Products

• 66417-49-0 (E)-3-(2,5-Diacetoxy-phenyl)-acrylic acid methyl ester 
• 583-69-7 2-bromobenzene-1,4-diol 
• 131136-47-5 2-Bromo-1,4-bis(methoxymethoxy)benzene 
• 22944-03-2 Siccayne 
• 131136-48-6 4-<2,5-Bis(methoxymethyloxy)phenyl>-2-methyl-3-butyn-2-ol 
• 827624-45-3 C₁₅H₁₈O₄Si 
• 636-70-4 triethylamine hydrobromide 
• 1233921-25-9 C₁₈H₁₄O₄ 

Relevant academic research and scientific papers

Total synthesis of (±)-ganocins B and C

The first total synthesis of structurally unique polycyclic phenolic meroterpenoids, ganocins B and C is reported. The synthesis features gold-catalyzed intramolecular cascade cyclization to construct the C/D ring bearing an angular methyl group, diastereoselective Michael addition, and acid-mediated one-pot Robinson cyclization/deprotection/isomerization.

SULPHONATE BASED COMPOUND, POLYMER ELECTROLYTE MEMBRANE COMPRISING SAME AND FUEL CELL COMPRISING SAME

The present invention relates to a novel sulfonate-based compound, a method for preparing the same, a polymer electrolyte membrane comprising the sulfonate-based compound, a membrane electrode assembly comprising the same and a fuel cell comprising the same.

Efficient synthesis of 5-nitro-benzo[b]furans via 2-bromo-4-nitro-phenyl acetates

Acetylation/Sonogashira cross-coupling reaction/cyclization has been carried out in one-pot using a Na2PdCl4/2-(di-tert-butylphosphino)-N-phenylindole/CuI system in TMEDA to give 5-nitro-2-substituted benzo[b]furans in excellent yields. We also describe the extension of this method to 4-EWG-2-bromo-phenols obtaining 2,5-disubstituted-benzo[b]furans in good yields.

LIQUID CRYSTAL COMPOUND COMPRISING TWO CONDENSED AND SUBSTITUTED RINGS

A new liquid crystal compound comprises two condensed and substituted rings. The ring preferably is a five-membered heterocyclic ring. The heterocyclic ring is preferably condensed with benzene ring or an aromatic six-membered heterocyclic ring. The benzene ring or the aromatic six-membered heterocyclic ring is preferably substituted with a group comprising a cyclic structure and a chain structure. The liquid crystal compound is advantageously used in preparation of a thin phase retarder, such as a wide-ranged l/4 plate, which gives inverse wavelength distribution. The phase retarder can be easily produced according to a simple process by using the new liquid crystal compound.

Formal total synthesis of shikonin via D?tz benzannulation

The D?tz benzannulation reaction provides mild conditions for the construction of highly functionalized aromatic compounds. We have utilized this method for the formal total synthesis of shikonin. The key step in our approach is the application of the D?tz benzannulation reaction between Fischer a chromium carbene complex and an optically active alkyne for the construction of the aromatic skeleton. This is followed by protecting group manipulation and formation of the epoxide moiety using the Sharpless procedure.