35086-59-0

Basic information

• Product Name: 3,5-Diacetoxyacetophenone
• Synonyms: 1-[3,5-Bis(acetyloxy)phenyl]-ethanone;3',5'-DIACETOXYACETOPHENONE;3,5-DIACETOXYACETOPHENONE;3',5'-DIACETYLOXYACETPHENONE;3-ACETYL-5-(ACETYLOXY)PHENYL ACETATE;5-ACETYL-1,3-PHENYLENE DIACETATE;3,5-Diacetoxyacetophonone;3',5'-Diacetoxyacetophenone 3-Acetyl-5-(Acetyloxy)phenyl Acetate
• CAS NO: 35086-59-0
• Molecular Formula: C₁₂H₁₂O₅
• Molecular Weight: 236.22068
• EINECS: 252-354-2
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);Building Blocks for Dendrimers;Functional Materials;Aromatics
• Mol File: 35086-59-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 91-94 °C(lit.)
• Boiling Point: 165-168 °C (0.7501 mmHg)
• Flash Point: 168.7 °C
• Appearance: yellow to brown powder
• Density: 1.3026 (rough estimate)
• Vapor Pressure: 6.63E-06mmHg at 25°C
• Refractive Index: 1.5140 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3,5-Diacetoxyacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Diacetoxyacetophenone(35086-59-0)
• EPA Substance Registry System: 3,5-Diacetoxyacetophenone(35086-59-0)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 9-21
• Hazardous Substances Data: 35086-59-0(Hazardous Substances Data)

Usage

Description

3,5-Diacetoxyacetophenone, with the CAS number 35086-59-0, is an organic compound that is characterized by its yellow to brown powdery appearance. It is a versatile molecule that finds applications in various fields due to its unique chemical properties.

Uses

Used in Organic Synthesis:
3,5-Diacetoxyacetophenone is used as an intermediate in the synthesis of various organic compounds. Its chemical structure allows for further functionalization and modification, making it a valuable building block in the creation of more complex molecules for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-Diacetoxyacetophenone is used as a key component in the development of new drugs. Its unique chemical properties enable it to be incorporated into the structures of potential therapeutic agents, contributing to their overall efficacy and safety.
Used in Chemical Research:
3,5-Diacetoxyacetophenone is also utilized in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic pathways. Its reactivity and structural features make it an ideal candidate for understanding the behavior of similar molecules in different chemical environments.
Used in Dye and Pigment Industry:
3,5-Diacetoxyacetophenone's color properties make it a potential candidate for use in the dye and pigment industry. 3,5-Diacetoxyacetophenone can be used as a starting material for the synthesis of various dyes and pigments, contributing to the development of new colorants with improved properties.

InChI:InChI=1/C12H12O5/c1-7(13)10-4-11(16-8(2)14)6-12(5-10)17-9(3)15/h4-6H,1-3H3

Upstream product

• 39192-49-9 3,5-diacetoxybenzoyl chloride 
• 506-82-1 dimethylcadmium 
• 75-36-5 acetyl chloride 
• 51863-60-6 3,5-dihydroxyacetophenone 
• 108-24-7 acetic anhydride 
• 676-58-4 methylmagnesium chloride 
• 99-10-5 3,5-Dihydroxybenzoic acid 

Downstream Products

• 51863-60-6 3,5-dihydroxyacetophenone 
• 144660-11-7 1-(3,5-diacetoxyphenyl)-2,2-dichloro-1-ethanone 
• 209746-95-2 1,3-diacetoxy-5-ethylbenzene 
• 62932-92-7 2-bromo-1-(3,5-dihydroxyphenyl)ethan-1-one 
• 847862-83-3 1-(1-hydroxyethyl)-3,5-diacetoxybenzene 
• 36763-39-0 3',5'-diacetyloxy-2-bromoacetophenone 
• 92637-51-9 C₁₂H₁₀Br₂O₅ 
• 53144-56-2 (R)‐5‐(2‐(tert‐butylamino)‐1‐hydroxyethyl)benzene‐1,3‐diol hydrochloride 
• 39878-43-8 2-chloro-1-(3,5-dihydroxy-phenyl)-ethanone 
• 81732-48-1 bis-3,5-(N,N-dimethylcarbamoyloxy)-acetophenone 

Relevant articles and documents

Preparation method of terbutaline sulphate

The invention relates to a preparation method of terbutaline sulphate. The technical problems that according to an existing preparation method of terbutaline sulphate, high-pressure hydrogenation and other high-risk operations, and lithium methide, azomethane and other high-risk reagents exist, and cost is high are solved through the preparation method. 3,5-resacetophenone serves as a raw material, and terbutaline sulphate is obtained through hydroxyl protection, the bromination reaction, carbonyl reduction, the condensation reaction and sulphating. The preparation method can be suitable for industrially-produced terbutaline sulphate.

PREPARATION METHOD OF ACYLBENZENES

A process for the production of acylbenzenes, comprising reacting diacetoxybenzoyl chloride with a Grignard reagent in the presence of an iron-containing catalyst. The acylbenzenes are useful intermediates in a multistep process for the preparation of resveratrol.