36441-29-9

Basic information

• Product Name: 14-phenyl-14H-dibenzo[a.j]xanthene
• Synonyms: 14-phenyl-14H-dibenzo[a.j]xanthene
• CAS NO: 36441-29-9
• Molecular Weight: 358.439
• Mol File: 36441-29-9.mol

Chemical Properties

• CAS DataBase Reference: 14-phenyl-14H-dibenzo[a.j]xanthene(CAS DataBase Reference)
• NIST Chemistry Reference: 14-phenyl-14H-dibenzo[a.j]xanthene(36441-29-9)
• EPA Substance Registry System: 14-phenyl-14H-dibenzo[a.j]xanthene(36441-29-9)

Safety Data

• Hazardous Substances Data: 36441-29-9(Hazardous Substances Data)

Upstream product

• 64-19-7 acetic acid 
• 40473-53-8 2-Hydroxy-1-(α-hydroxybenzyl)naphthalene 
• 135-19-3 β-naphthol 
• 64-17-5 ethanol 
• 98-07-7 Benzotrichlorid 
• 98-87-3 benzylidene dichloride 
• 54533-84-5 2-(2-(2-chloroethoxy)ethoxy)tetrahydro-2H-pyran 
• 29114-24-7 benzylidene-1,1'-bis(2-naphthol) 
• 7647-01-0 hydrogenchloride 
• 219897-32-2 1-(α-aminobenzyl)-2-naphthol hydrochloride 
• 6642-31-5 6-Amino-1,3-dimethylbarbituric acid 
• 100-52-7 benzaldehyde 
• 100-01-6 4-nitro-aniline 
• 100-51-6 benzyl alcohol 

Downstream Products

• 294627-85-3 14-phenyl-14H-dibenzo[a,j]xanthenylium bromide 
• 116468-94-1 14-hydroxy-14-phenyldibenzo[a,j]xanthene 
• 460-35-5 3-chloro-1,1,1-trifluoropropane 
• 460-69-5 1,1-dichloro-3,3,3-trifluoropropane 
• 7125-84-0 1,1,1-trichloro-3,3,3-trifluoropropane 
• 530740-47-7 1-(4-chloro-1-hydroxy-2-naphthyl)ethanone 
• 2612-57-9 2,4-dichlorophenyl isocyanate 
• 624-96-4 1,3-dichloro-3-methylbutane 
• 616-13-7 1-chloro-2-methylbutane 
• 507-45-9 2,3-dichloro-2-methylbutane 
• 623-34-7 1,4-dichloro-2-methylbutane 
• 4400-06-0 3,4',5-trichloro-4-hydroxybiphenyl 
• 715-34-4 methyl 3,5-dichloro-2,4-dihydroxy-6-methylbenzoate 

Relevant articles and documents

Facile montmorillonite K-10-supported synthesis of xanthene derivatives under microwave and thermal conditions

Microwave-assisted and thermal condensations of aromatic and aliphatic aldehydes with β-naphthol adsorbed onto montmorillonite K-10 were conducted in a one-pot procedure leading to the formation of a variety of xanthene derivatives. Under microwave irradi

1,3-Dibromo 5,5-dimethylhydantoin (DBH): A novel and efficient catalyst for the synthesis of 14-aryl-14H-dibenzo[a, j] xanthenes under solvent-free conditions

An atom-efficient and environment-friendly approach for the synthesis of aryl-14H-dibenzo[a,j]xanthenes (3a-o) via the one-pot reaction of β-naphthol and aryl aldehydes (1) catalyzed by DBH has been developed. The present approach offers several advantage

Cation-exchange resins: Efficient heterogeneous catalysts for facile synthesis of dibenzoxanthene from β-naphthol and aldehydes

β-Naphthol reacts with alkyl and aryl aldehydes in the presence of Indion-130 to give 14-alkyl/aryl-14H[ a,j ]dibenzoxanthenes in good yield. Copyright Taylor & Francis Group, LLC.

Synthesis of 14H-dibenzo xanthene derivatives using choline chloride/tin(II) chloride deep eutectic solvent and Fe3O4/?-carrageenan/Zn(II)

In this study, various xanthene derivatives have prepared efficiently through a simple method using choline chloride/tin(II) chloride (ChCl·2SnCl2) deep eutectic solvent (DES), alone, or in the presence of Fe3O4/?-carragee

Efficient synthesis of aryl-14H-dibenzo[a.j]xanthenes using NaHSO4-SiO2 or 5%WO3/ZrO2 as heterogeneous catalysts under conventional heating in a solvent-free media

A simpler and greener protocol has been developed for the preparation of aryl-14H-dibenzo[a.j]xanthenes: a one-pot condensation of β-naphthol and aryl aldehydes, in the presence of silica-supported sodium hydrogen sulfate (NaHSO4·SiO2) or tungstated zirco

Synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes catalyzed by acyclic acidic ionic liquids

Some recyclable acyclic SO3H-functionalized ionic liquids have been used as novel catalysts for the synthesis of 14-aryl-14H-dibenzo[a,j] xanthenes via the one-pot condensation of β-naphthol and aromatic aldehydes in aqueous medium. The condens

BF3·SiO2: an efficient alternative for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes

Silica-supported boron trifluoride (BF3·SiO2) is an efficient, readily available, and reusable catalyst for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes by condensation of 2-naphthol and aldehydes. This reaction under

A clean, mild, and efficient preparation of aryl 14H-benzo[a,j]xanthene leuco-dye derivatives via nanocatalytic MCM-41-SO3h under ultrasonic irradiation in aqueous media

Aim and Objective: The present study has developed an efficient and eco-friendly protocol for the synthesis of aryl-14-H-dibenzo[a,j] xanthenes through a one-pot condensation reaction of 2-naphthol and arylaldehydes in aqueous media using the nanocatalyti

A simple and efficient one-pot bis-bromine-1,4-diazabicyclo [2.2.2]octane (Br2-DABCO) catalyzed synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under solvent-free conditions

Bis-bromine-1,4-diazabicyclo[2.2.2]octane (Br2-DABCO) is an efficient, readily available, and reusable catalyst for the synthesis of 14-aryl-14 H-dibenzo[a,j]xanthenes 3 by condensation of β-naphthol 2 and aldehydes 1. This reaction under solve

Design, synthesis and antiviral potential of 14-aryl/heteroaryl-14H- dibenzo[a, j]xanthenes using an efficient polymer-supported catalyst

Polyethyleneglycol bound sulfonic acid (PEG-OSO3H), a chlorosulphonic acid-modified polyethylene glycol was successfully used as an efficient and eco-friendly polymeric catalyst in the synthesis of 14-aryl/heteroaryl-14H-dibenzo[a, j]xanthenes