909389-74-8

Basic information

• Product Name: acetic acid 3,5-dibromo-phenyl ester
• Synonyms: acetic acid 3,5-dibromo-phenyl ester
• CAS NO: 909389-74-8
• Molecular Formula: C₈H₆Br₂O₂
• Molecular Weight: 293.94004
• EINECS: -0
• Mol File: 909389-74-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: acetic acid 3,5-dibromo-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: acetic acid 3,5-dibromo-phenyl ester(909389-74-8)
• EPA Substance Registry System: acetic acid 3,5-dibromo-phenyl ester(909389-74-8)

Safety Data

• Hazardous Substances Data: 909389-74-8(Hazardous Substances Data)

Upstream product

• 626-41-5 3,5-dibromophenol 
• 108-22-5 Isopropenyl acetate 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 108-36-1 1,3-dibromobenzene 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 669767-20-8 2',4'-dibromo-6'-hydroxyacetophenone 
• 1423702-17-3 C₉H₈Br₂O₂ 
• 1423702-20-8 C₉H₉Br₂NO₂ 
• 1423702-22-0 C₉H₈BrNO₂ 
• 1423702-25-3 C₈H₆BrNO₂ 
• 1423702-28-6 C₁₈H₁₇NO₄ 
• 1423702-31-1 C₁₉H₁₆F₃NO₆S 
• 1423702-34-4 C₁₈H₁₈N₂O₃ 
• 1423690-66-7 C₂₇H₂₅ClN₂O₅ 
• 1423684-81-4 C₂₅H₂₁ClN₂O₅ 
• 918826-08-1 3,5-diethynyl-phenol 
• 1020182-87-9 3,5-bis((trimethylsilyl)ethynyl)phenyl acetate 

Relevant articles and documents

Molecular architecture via coordination: Self-assembly of nanoscale hexagonal metallodendrimers with designed building blocks

The first self-assembly of nanoscale metallodendrimers that have a hexagonal cavity as a core via the directional-bonding approach is reported. All metallodendrimers were characterized by multinuclear NMR (1H and 31P), mass spectrome

Orthogonal Self-Assembly of a Two-Step Fluorescence-Resonance Energy Transfer System with Improved Photosensitization Efficiency and Photooxidation Activity

During the past few decades, fabrication of multistep fluorescence-resonance energy transfer (FRET) systems has become one of the most attractive topics within supramolecular chemistry, chemical biology, and materials science. However, it is challenging t

Protection of COOH and OH groups in acid, base and salt free reactions

We report an iron-catalyzed general functional group protection method with inexpensive reagents. This environmentally benign process does not use acids or bases, and does not produce waste products. Further purification beyond filtration and evaporation is, in most cases, unnecessary. Free COOH and OH groups can be protected in a one-pot reaction.

Ligand-Promoted Palladium-Catalyzed C?H Acetoxylation of Simple Arenes

The palladium-catalyzed C?H oxidation of simple arenes is an attractive strategy to obtain phenols, which have many applications in the fine chemicals industry. Although some advances have been made in this research area, low reactivity and selectivity are, in general, observed. This report describes a new catalytic system for the efficient C?H acetoxylation of simple arenes based on Pd(OAc)2 and a pyridinecarboxylic acid ligand.