144152-28-3

Basic information

• Product Name: Ethanone, 1-[2,6-bis(acetyloxy)phenyl]-
• CAS NO: 144152-28-3
• Molecular Formula: C12H12O5
• Molecular Weight: 236.224
• Mol File: 144152-28-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2,6-bis(acetyloxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2,6-bis(acetyloxy)phenyl]-(144152-28-3)
• EPA Substance Registry System: Ethanone, 1-[2,6-bis(acetyloxy)phenyl]-(144152-28-3)

Safety Data

• Hazardous Substances Data: 144152-28-3(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-[2,6-bis(acetyloxy)phenyl]- is a compound that belongs to the class of organic chemicals known as benzophenones. It is commonly used in the production of sunscreens and hair care products due to its ability to absorb and filter ultraviolet (UV) light. This chemical is a derivative of benzophenone, which is known for its photoprotective properties. Its structure contains two acetyloxy groups attached to a phenyl ring, providing enhanced UV protection capabilities. Overall, Ethanone, 1-[2,6-bis(acetyloxy)phenyl]- is a valuable ingredient in various cosmetic and skincare formulations for its UV-blocking properties.

Upstream product

• 699-83-2 2,6-dihydroxylacetophenone 
• 108-24-7 acetic anhydride 

Downstream Products

• 26239-18-9 3-acetyl-5-hydroxy-2-methyl-4H-1-benzopyran-4-one 
• 444711-04-0 2-bromo-1-(2,6-diacetoxy-phenyl)-ethanone 
• 699-83-2 2,6-dihydroxylacetophenone 
• 26674-05-5 acetic acid 2-acetyl-3-hydroxyphenyl ester 
• 144822-82-2 4-hydroxy-2,3-dihydrobenzofuran 
• 24389-49-9 4-hydroxy-2-((Z)-4-hydroxy-benzylidene)-benzofuran-3-one 
• 19278-81-0 4-hydroxy-1-benzofuran-3(2H)-one 

Relevant articles and documents

Synthesis of substituted 2,3-dihydrobenzofuran in a process involving a facile acyl migration

Reduction of 2,6-diacetoxy-2′-bromoacetophenone (10) with NaBH4 led to 3,4-diacetoxydihydrobenzofuran (12) in a process involving acyl migration followed by cyclization. Subsequent hydrogenolysis gave 4-acetoxydihydrobenzofuran which, upon saponification, afforded 4-hydroxydihydrobenzofuran (8) in good yield. This approach is shown to be a general method for preparation of substituted dihydrobenzofurans.

A method of cosmetic depigmentation care by applying at least one aurone

At least one aurone or a natural or synthetic derivative of aurone, or an analogue of aurone, in which the independent phenyl ring can be substituted by a heterocycle of pyrrole, imidazole, triazole, pyridine, furan, or thiophene type, is disclosed as a cosmetic agent, or as an active substance, for the manufacture either of a cosmetic composition, or of a pharmaceutical composition, notably a dermatological composition, having a melanogenesis-inhibiting activity or a depigmenting activity, or an anti-tyrosinase activity.