4004-51-7

Basic information

• Product Name: 1-Naphthol,phosphate
• Synonyms: 1-Naphthol, phosphate;1-Naphthol,phosphate;Tri-α-naphthyl phosphate
• CAS NO: 4004-51-7
• Molecular Formula: C₃₀H₂₁O₄P
• Molecular Weight: 0
• Mol File: 4004-51-7.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Naphthol,phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthol,phosphate(4004-51-7)
• EPA Substance Registry System: 1-Naphthol,phosphate(4004-51-7)

Safety Data

• Hazardous Substances Data: 4004-51-7(Hazardous Substances Data)

Usage

InChI:InChI=1S/C30H21O4P/c31-35(32-28-19-7-13-22-10-1-4-16-25(22)28,33-29-20-8-14-23-11-2-5-17-26(23)29)34-30-21-9-15-24-12-3-6-18-27(24)30/h1-21H

Upstream product

• 90-15-3 α-naphthol 
• 10026-13-8 phosphorus pentachloride 
• 10025-87-3 trichlorophosphate 
• 86-48-6 1-hydroxy-2-naphthoic acid 
• 13869-17-5 tris(1-naphthyl) phosphite 
• 3019-88-3 sodium naphtholate 

Downstream Products

• 90-15-3 α-naphthol 
• 124-38-9 carbon dioxide 
• 34160-17-3 1-(N-methyl-N-phenylamino)-naphthalene 
• 98223-72-4 N-(1-naphthyl)morpholine 
• 604-53-5 1,1'-binaphthalene radical cation 
• 604-53-5 1,1'-bisnaphthalene 
• 1136-89-6 1-naphthylphosphoric acid 
• 116346-04-4 1,2'-binaphthalene-1'-ol 
• 17752-78-2 dimethyl 1-naphthyl phosphate 
• 3264-24-2 7H-dibenzoxanthen-7-one 
• 86-53-3 1-Cyanonaphthalene 

Relevant articles and documents

Lead ion induced chemodosimeter approach of a tripodal hydroxyl-quinoline based phospho-ester through P-O bond cleavage

Lead ion induced P-O bond breaking with instant colour change was observed in a tripodal hydroxyl-quinoline based phosphor-ester (HQP). A new penta-coordinated lead chelate complex [Pb4HQ6(ClO4)2] was found. The hydrolysis reaction followed by P-O bond cleavage with 'Pb-O' and 'Pb-N' bond formation proved the chemodosimeter approach.

Microwave-assisted synthesis of triaryl phosphates

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Polymer supported reagents: An efficiant and simple method for the synthesis of triaryl phosphates

The reaction of phosphoryl chloride with insoluble polymer-supported phenoxide ion reagents in benzene at room temperature, produced triaryl phosphates in excellent yields. The isolation of pure products by simple filtration and evaporation is an important feature of this method.