606-12-2

Usage

Uses

Used in Nanocomposite Material Industry:
2,4'-Dihydroxybenzophenone is used as a key component in the preparation method for anti-fog and antibacterial coatings of nanocomposite materials. Its unique properties contribute to the development of advanced coatings with improved performance characteristics, such as reduced fogging and enhanced antibacterial properties, making them suitable for various applications, including automotive, architectural, and personal protective equipment industries.

Preparation

Preparation by diazotization of 2,4′ -diamino- 2′,4-di-hydroxybenzophenone, followed by decomposition of the diazonium salt obtained in the presence of 50% hypo-phosphorous acid (57%).

InChI:InChI=1/C13H10O3/c14-10-7-5-9(6-8-10)13(16)11-3-1-2-4-12(11)15/h1-8,14-15H

Upstream product

• 5449-69-4 2,4'-dimethoxybenzophenone 
• 68223-20-1 (2-hydroxyphenyl)(4-nitrophenyl)methanone 
• 861358-09-0 9-(4-hydroxy-phenyl)-xanthen-3-one 
• 959033-36-4 (2-acetoxy-phenyl)-(4-acetoxy-phenyl)-methane 
• 2037-19-6 3-(2-hydroxy-phenyl)-3-(4-hydroxy-phenyl)-phthalide 
• 14963-42-9 2,4'-diamino-benzophenone 
• 118-55-8 phenyl Salicylate 
• 69-72-7 salicylic acid 
• 108-95-2 phenol 
• 56-23-5 tetrachloromethane 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 113272-16-5 (1α,4aβ,9aβ)-1,2,4a,9a-tetrahydro-1-methoxy-3,9-dioxo-4H-xanthene-9a-carboxaldehyde 
• 113272-11-0 (8aR,10aR)-8-Methoxy-9-oxo-6-trimethylsilanyloxy-5,10a-dihydro-8H,9H-xanthene-8a-carbaldehyde 
• 7646-78-8 tin(IV) chloride 

Downstream Products

• 108-95-2 phenol 
• 99-96-7 4-hydroxy-benzoic acid 
• 6272-13-5 2,4'-Dihydroxy-benzhydrol 
• 5333-67-5 2,4'-Diacetoxybenzophenone 
• 5449-69-4 2,4'-dimethoxybenzophenone 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 31772-32-4 [2-(6-Bromo-hexyloxy)-phenyl]-(4-hydroxy-phenyl)-methanone 
• 31772-31-3 [2-(6-Bromo-hexyloxy)-phenyl]-(4-methoxymethoxy-phenyl)-methanone 

Relevant academic research and scientific papers

Selective Oxidation of Alkylarenes to the Aromatic Ketones or Benzaldehydes with Water

Here a palladium-catalyzed oxidation method for converting alkylarenes into the aromatic ketones or benzaldehydes with water as the only oxygen donor is reported. This C-H bond oxidation functionalization does not require other oxidants and hydrogen accep

4,4′-Benzophenone-O,O′-disulfamate: A potent inhibitor of steroid sulfatase

We investigated whether the benzophenone moiety can be used as core element of steroid sulfatase (STS) inhibitors. While 4- and 3-benzophenone-O-sulfamates inhibit STS with IC50 values between 5 and 7 μM irrespective of additional hydroxy and m

Cycloadditions of substituted benzopyran-4-ones to electron-rich dienes: a new route to xanthone derivatives

The benzopyranones 1 and 3 reacted with 2,3-dimethyl-1,3-butadiene in the presence of titanium (IV) chloride to give the corresponding (4 + 2) cycloadducts 8 and 11, the former undergoing facile deformylation to give 9 and 10. Compounds 1, 3, and 4 underwent efficient uncatalysed cycloaddition to 1- methoxy-3-(trimethylsilyloxy)-l,3-butadiene 12 to give the respective adducts 13,14, and 18 as mixtures of C-l stereoisomers. Heating the 3-arylsulphinylchromone 5 with the diene 12 afforded 3-hydroxyxanthone 23 in 50% yield, the presumed cycloaddition - elimination sequence constituting a new route to xanthone systems. Desilylation of 13,14, and 18 in acidic media provided 25,26, and 27 respectively.

Production of hydroxy arylophenones

Production of a hydroxy arylophenone by reacting an aromatic carboxylic acid Ar(--CO2 H)p where Ar is an aromatic radical, (--CO2 H) is an aromatic carboxylic acid group, and p is 1 or 2 with an aromatic compound H--Ar'--OH where Ar' is an aromatic radical and --H and --OH are aromatically bound para to each other in a benzenoid ring, in the presence of an alkyl sulphonic acid, particularly methane sulphonic acid, to produce a hydroxy arylophenone of formula Ar(--CO--Ar'--OH)p where the carbonyl and hydroxyl groups are para to each other in the hydroxyl-containing benzenoid ring of Ar'. The production of the hydroxy arylophenone proceeds through the intermediate ester (H--Ar'--O--CO--)p Ar and the production of the hydroxy arylophenone starting from the ester is also claimed.