36041-39-1

Basic information

• Product Name: 2-Benzoyl-p-benzoquinone
• Synonyms: 2-Benzoyl-1,4-benzoquinone;2-Benzoyl-p-benzoquinone
• CAS NO: 36041-39-1
• Molecular Formula: C₁₃H₈O₃
• Molecular Weight: 0
• Mol File: 36041-39-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Benzoyl-p-benzoquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Benzoyl-p-benzoquinone(36041-39-1)
• EPA Substance Registry System: 2-Benzoyl-p-benzoquinone(36041-39-1)

Safety Data

• Hazardous Substances Data: 36041-39-1(Hazardous Substances Data)

Upstream product

• 106-51-4 p-benzoquinone 
• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 14770-96-8 oxybenzone 
• 150-78-7 1,4-dimethoxybezene 
• 98635-85-9 (2,5-dimethoxyphenyl)(phenyl)methanol 
• 4038-13-5 2,5-dimethoxybenzophenone 
• 10034-85-2 hydrogen iodide 
• 2050-37-5 2,5-dihydroxybenzophenone 

Downstream Products

• 94797-63-4 4a,8a-cis-4a,5-trans-5-acetoxy-4a-benzoyl-4a,5,8,8a-tetrahydro-1,4-naphthoquinone 
• 94797-61-2 4a,8a-cis-2-benzoyl-4a,5,8,8a-tetrahydro-1,4-naphthoquinone 
• 1314873-32-9 6-phenyl-8-phenylamino-3,4-dihydrophenanthridine-1,7,10(2H)-trione 
• 1314873-19-2 C₁₉H₁₃NO₃ 
• 94797-70-3 2-benzoyl-5,8-dihydro-6,7-dimethylnaphthalene-1,4-diol 
• 94797-68-9 (1,4-dihydroxy-2-naphthyl)(phenyl)methanone 
• 112450-22-3 4-benzoyl-5-hydroxy-1,3-benzoxathiol-2-one 
• 78606-54-9 2-benzoyl-5,8-dihydro-8-methylnaphthalene-1,4-diol 
• 420782-25-8 ethyl 3-phenyl-4,7-dioxo-4,7-dihydrobenzo[b]thiophene-2-carboxylate 

Relevant articles and documents

Half-wave potentials and in vitro cytotoxic evaluation of 3-acylated 2,5-bis(phenylamino)-1,4-benzoquinones on cancer cells

A broad range of 3-acyl-2,5-bis(phenylamino)-1,4-benzoquinones were synthesized and their voltammetric values, as well as in vitro cancer cell cytotoxicities, were assessed. The members of this series were prepared from acylbenzoquinones and phenylamines, in moderate to good yields (47-74%), through a procedure involving a sequence of two in situ regioselective oxidative amination reactions. The cyclic voltammograms of the aminoquinones exhibit two one-electron reduction waves to the corresponding radical-anion and dianion, and two quasi-reversible oxidation peaks. The first and second half-wave potential values (E1/2) of the members of the series were sensitive to the push-pull electronic effects of the substituents around the benzoquinone nucleus. The in vitro cytotoxic activities of the 3-acyl-2,5-bis(phenylamino)-1,4-benzoquinones against human cancer cells (bladder and prostate) and non-tumor human embryonic kidney cells were measured using the MTT colorimetric method. The substitution of both aniline groups, by either methoxy (electron donating effect) or fluorine (electron withdrawal effect), decreased the cytotoxicity in the aminoquinones. Among the members of the unsubstituted phenylamino series, two of the 18 compounds showed interesting anti-cancer activities. A preliminary assay, looking for changes in the expression of selected genes, was performed. In this context, the two compounds increased TNF gene expression, suggesting an association with an inflammatory-like response.

Studies on quinones. Part 47. Synthesis of novel phenylaminophenanthridinequinones as potential antitumor agents

In our search for potential anticancer agents, a series of 8- and 9-phenylamino-3,4-tetrahydro-phenanthridine-1,7,10(2H)-triones with substituent variations at 6-, 8- and 9-positions were prepared using a highly efficient sequence involving: a) solar photoacylation reactions of benzoquinone with arylaldehydes, b) one-pot procedure for the synthesis of 3,4- dihydrophenanthridine-1,7,10(2H)-trione intermediates from acylhydroquinones and c) highly regiocontrolled acid-induced amination reaction of phenanthridinequinones with phenylamines. The members of this series were in vitro evaluated using the MTT colorimetric method against one normal cell line and three human cancer cell lines. The SAR analysis indicates that the location of nitrogen substituents on the quinone nucleus, the presence of methyl, phenyl, furyl and thienyl groups at the 6-position and the aromatization of the angular cycloaliphatic ring of the phenylamino-3,4-tetrahydrophenanthridine-1,7,10(2H)- trione pharmacophore play key roles in the antitumor activity.

An improved method for the preparation of 4,7-Dioxo-4,7-dihydrobenzo[b]thiophene-2-carboxylates from 2-acyl-1,4-benzoquinones and mercaptoacetates

4,7-Dioxo-4,7-dihydrobenzo[b]thiophene-2-carboxylates (4) have been synthesized in a one-pot procedure from 2-acyl-1,4-benzoquinones (1) and mercaptoacetates (2) by using 1-trimethylsilylimidazole as a protective reagent as well as a base. Thus, reaction of 1 with 2 in THF at room temperature was followed by treatment with excess of 1-trimethylsilylimidazole at 80°C. Then the cooled mixture was hydrolyzed with hydrochloric acid and oxidized with cerium(IV) ammonium nitrate (CAN) to give the expected thiophenequinone derivatives (4). 4,9-Dioxo-4,9-dihydronaphtho[2,3-b]thiophene-2-carboxylates (7) were similarly prepared from 2-acyl-1,4-naphthoquinones (5) and mercaptoacetates, in general, by omitting the CAN oxidation procedure.

Action regioselective du nitrate d'ammonium et de cerium(IV) sur quelques isobenzofurannequinones et sur le dimethoxy-4,7 diphenyl-1,3 benzothiophene

Cerium ammonium nitrate (CAN) oxidized furanquinones 4c, 4d and 7 to diketonic quinones 5c, 5d and 8 but does not react with quinone 4e; it oxidizes the dimethoxyisobenzothiophene 2b into the quinone 1, but the photooxidation of the compound 2b gives the

STUDIES ON QUINONES XVII. THE REACTION OF ACYLBENZOQUINONES WITH HYDRAZOIC ACID: A ROUTE TO THE PREPARATION OF 2,1-BENZISOXAZOL-4,7-QUINONES

A straightforward route to 2,1-benzisoxazol-4,7-quinones by oxidation of acylazido hydroquinones, obtained through reaction of acylbenzoquinones with hydrazoic acid, is described.