1985-37-1

Basic information

• Product Name: 1-PHENYL-2 3-NAPHTHALENEDICARBOXYLIC
• Synonyms: 1-PHENYL-2 3-NAPHTHALENEDICARBOXYLIC;NSC17350
• CAS NO: 1985-37-1
• Molecular Formula: C₁₈H₁₀O₃
• Molecular Weight: 274.274
• Product Categories: P;Stains and Dyes;Stains&Dyes, A to
• Mol File: 1985-37-1.mol
• Article Data: 10

Chemical Properties

• Melting Point: 259-262 °C(lit.)
• Boiling Point: 489.8°Cat760mmHg
• Flash Point: 246.7°C
• Appearance: /
• Density: 1.358g/cm³
• Vapor Pressure: 9.64E-10mmHg at 25°C
• Refractive Index: 1.7
• CAS DataBase Reference: 1-PHENYL-2 3-NAPHTHALENEDICARBOXYLIC(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PHENYL-2 3-NAPHTHALENEDICARBOXYLIC(1985-37-1)
• EPA Substance Registry System: 1-PHENYL-2 3-NAPHTHALENEDICARBOXYLIC(1985-37-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 1985-37-1(Hazardous Substances Data)

Usage

Uses

1-Phenyl-2,3-naphthalenedicarboxylic anhydride is a polyaromatic small molecule dye. Dyes and metabolites.

InChI:InChI=1/C18H10O3/c19-17-14-10-12-8-4-5-9-13(12)15(16(14)18(20)21-17)11-6-2-1-3-7-11/h1-10H

Upstream product

• 16269-23-1 (3E, 4E)-3,4-dibenzylidenedihydrofuran-2,5-dione 
• 108-31-6 maleic anhydride 
• 131-58-8 2-Methylbenzophenone 
• 7063-23-2 phenylpropiolic acid sodium salt 
• 1885-14-9 phenyl chloroformate 
• 637-44-5 phenylpropyolic acid 
• 71-43-2 benzene 
• 7299-58-3 phenylpropiolyl chloride 
• 501-52-0 3-Phenylpropionic acid 
• 538-75-0 dicyclohexyl-carbodiimide 
• 75057-14-6 N-hydroxy-1-phenylnaphthalene-2,3-dicarboximide 

Downstream Products

• 75258-83-2 4-phenyl-1H-benzo[f]isoindole-1,3(2H)-dione 
• 565472-27-7 ethyl 3-(1,3-dioxo-4-phenyl-1,3-dihydro-benzo[f]isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate 
• 82089-99-4 tetra-1-phenylnaphthalocyanine vanadyl complex 
• 59883-21-5 2,3-bis(hydroxymethyl)-1-phenylnaphthalene 
• 50558-51-5 4-phenylnaphtho[2,3-c]firan-1(3H)-one 
• 75258-80-9 2-(1,3-Dioxo-4-phenyl-1,3-dihydro-benzo[f]isoindol-2-yl)-benzoic acid 
• 75258-82-1 4-(1,3-Dioxo-4-phenyl-1,3-dihydro-benzo[f]isoindol-2-yl)-benzoic acid 
• 75258-81-0 3-(1,3-Dioxo-4-phenyl-1,3-dihydro-benzo[f]isoindol-2-yl)-benzoic acid 
• 21867-10-7 5-phenyl-1,2,3,4-tetrahydrobenzophthalazine-1,4-dione 
• 22290-93-3 N-phenyl-1-phenyl-naphthalene-2,3-dicarboximide 
• 68775-42-8 2-(4-methoxy-phenyl)-4-phenyl-benzo[f]isoindole-1,3-dione 
• 31996-14-2 N-anilino-1-phenylnaphthalene-2,3-dicarboximide 
• 62604-90-4 4-phenyl-2-p-tolyl-benzo[f]isoindole-1,3-dione 
• 52905-36-9 7H-benzofluoren-7-one-6-carboxylic acid 

Relevant articles and documents

One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1, 3(2H)-diones by T3P activation of 3-arylpropiolic acids

In situ activation of 3-arylpropiolic acids with T3P (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2, 3-c]furan-1, 3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue-lumi

1-phenyl -2,3-naphthalene carboxylic acid anhydride, and its process for synthesis of derivatives of

The invention discloses a synthesis method of 1-phenyl-2,3-naphthalene dicarboxylic anhydride and derivatives thereof. The synthesis method is used for synthesizing the 1-phenyl-2,3-naphthalene dicarboxylic anhydride compounds under an alkali condition in

Phthalocyanines and related compounds: XXXIX. Synthesis of derivatives of some substituted 1-phenylnaphthalene-2,3-dicarboxylic acids

Derivatives (dinitriles, anhydrides, imides, N-phenylimides) of substituted 1-phenylnaphthalene-2,3-dicarboxylic and 1-phenylphenanthrene-2,3-dicarboxylic acids were prepared by the reactions of 2-bromomethylbenzophenones with various dienophiles. Starting from these derivatives, gallium complexes of substituted tetra-1-phenyl-2,3-naphthalocyanines and tetra(1-phenyl-2,3-phenanthro) porphyrazine were synthesized. 2005 Pleiades Publishing, Inc.