19419-25-1

Basic information

• Product Name: 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-
• Synonyms: 9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione;1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-
• CAS NO: 19419-25-1
• Molecular Formula: C₂₄H₂₈O₄
• Molecular Weight: 380.48
• Mol File: 19419-25-1.mol
• Article Data: 117

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-(19419-25-1)
• EPA Substance Registry System: 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-(19419-25-1)

Safety Data

• Hazardous Substances Data: 19419-25-1(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 126-81-8 dimedone 
• 504-02-9 1,3-cylohexanedione 
• 63-74-1 sulfanilamide 
• 591-31-1 3-methoxy-benzaldehyde 
• 7560-94-3 2,2'-((4-methoxyphenyl)methylene)bis(3-hydroxy-5,5-dimethylcyclohex-2-enone) 
• 100-46-9 benzylamine 
• 3585-93-1 N-(4-methoxybenzylidene)aniline oxide 
• 165263-70-7 C₁₁H₁₂N₄O 
• 135-19-3 β-naphthol 
• 49546-71-6 5-(4-methoxybenzylidene)barbituric acid 
• 15485-22-0 4-chloro-N-[(4-methoxyphenyl)methylidene]aniline 
• 57-13-6 urea 
• 19419-24-0 2,2′-(4-methoxyphenylmethylene)bis(3-hydroxy-5,5′-dimethyl cyclohexane-1,3-dione) 

Downstream Products

• 1437314-29-8 C₂₄H₂₈N₈O₂ 
• 889-31-6 5,5-dimethyl-3-benzylamino-2-cyclohexen-1-one 
• 126-81-8 dimedone 
• 155333-73-6 2-Methoxy-5-(3,3,6,6-tetramethyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)-benzenesulfonyl chloride 

Relevant articles and documents

A Rapid Ultrasound Synthesis of Xanthenediones Catalyzed by Boric acid in Ethanol-Water Medium: Single Crystal, DFT and Hirshfeld Surface Analysis of Two Representative Compounds

A highly versatile and efficient ultrasound promoted synthesis of xanthenedione derivatives is achieved through condensation of dimedone with various aromatic aldehydes using boric acid as catalyst in ethanol-water medium. The advantages of this method be

ChCl: Gly (DESs) promote environmentally benign synthesis of xanthene derivatives and their antitubercular activity

A ChCl: Gly (DESs) promoted environmentally benign method was developed for the first time using the reaction of aryl aldehydes and dimedone to give excellent yields of xanthene analogues. The major application of this present protocol is the use of green

Solvent influence upon complex formation between different 1,8-dioxo-octahydroxanthene derivatives and yttrium(III) cation in some non-aqueous solvents using conductometric method

The complexation reactions between the yttrium(III) cation and (4-chlorophenyl, phenyl, 4-nitrophenyl, 4-methoxyphenyl, 4-methylphenyl) 9-substituted 1,8-dioxo-octahydroxanthene were studied in acetonitrile (AN) and methanol (MeOH) at different temperatur

Phosphosulfonic acid, an efficient solid acid catalyst for the one-pot preparation of 14-aryl-14H-dibenzo[a,j]xanthenes and 1,8-dioxooctahydroxanthenes under solvent-free conditions

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[HSO4] catalyzed efficient and green synthesis of 1,8-dioxo-octahydroxanthenes

A simple and efficient procedure for synthesis of 1,8-dioxo- octahydroxanthenes by one-pot condensation of aromatic aldehydes with 5,5-dimethyl-1,3-cyclohexanedione under solvent-free conditions using ionic liquid [Et3NH][HSO4] as catalyst is described. The procedure offers several advantages including cleaner reaction profiles, use of easily available, cheap, recyclable and environmentally benign nature of catalyst, high yields, and simple experimental and work-up procedures.

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