47568-49-0

Basic information

• Product Name: 1,1'-BIS(2-HYDROXY-3-NAPHTHOIC ACID)
• Synonyms: 1,1'-BIS(2-HYDROXY-3-NAPHTHOIC ACID)
• CAS NO: 47568-49-0
• Molecular Formula: C₂₂H₁₄O₆
• Molecular Weight: 374.34
• Mol File: 47568-49-0.mol
• Article Data: 18

Chemical Properties

• Melting Point: 331-333 °C
• Boiling Point: 570.0±50.0 °C(Predicted)
• Appearance: /
• Density: 1.528±0.06 g/cm3(Predicted)
• PKA: 2.42±0.30(Predicted)
• CAS DataBase Reference: 1,1'-BIS(2-HYDROXY-3-NAPHTHOIC ACID)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-BIS(2-HYDROXY-3-NAPHTHOIC ACID)(47568-49-0)
• EPA Substance Registry System: 1,1'-BIS(2-HYDROXY-3-NAPHTHOIC ACID)(47568-49-0)

Safety Data

• Hazardous Substances Data: 47568-49-0(Hazardous Substances Data)

Usage

Family

Naphthalene derivatives

Type

Dihydroxynaphthalene carboxylic acid

Function

Complexing agent in metal chelates formulation

Ability

Forms stable complexes with metal ions

Industrial Applications

Dyes, pigments, and catalysts

Chelating Properties

Suitable for metal-based drugs and detection reagent in analytical chemistry

Intermediate

Used in the synthesis of other organic compounds

Potential Applications

Medicine and materials science

Upstream product

• 47644-69-9 dimethyl 2,2'-dihydroxy-1,1'-binaphthalene-3,3'-dicarboxylate 
• 18531-92-5 2,2'-dihydroxy-1,1'-binaphthalene-3,3'-dicarboxylic acid 
• 74292-20-9 (S)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl 
• 18531-99-2 (S)-[1,1']-binaphthalenyl-2,2'-diol 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 883-99-8 3-hydroxy-2-naphthoic acid methyl ester 
• 602-09-5 1,1'-bi-2-naphthol 
• 173831-50-0 rac-2,2'-bis-(methoxymethoxy)-1,1'-binaphthalene 
• 497106-69-1 (S)-1-(3-hydroxy-2-naphthylcarbonyl)pyrrolidine-2-carboxylic acid methyl ester 
• 1734-00-5 3-hydroxy-2-naphthoyl chloride 
• 7705-08-0 iron(III) chloride 
• 64-19-7 acetic acid 
• 7732-18-5 water 
• 64-17-5 ethanol 

Downstream Products

• 1398114-28-7 C₃₆H₂₈N₂O₄ 
• 18531-92-5 (S)-2,2'-dihydroxy-[1,1'-binaphthalene]-3,3'-dicarboxylic acid 
• 309269-73-6 (S)-3,3′-bis[hydroxy(diphenyl)methyl]-1,1′-binaphthalene-2,2′-diol 

Relevant articles and documents

PROCESS FOR POLYMERIZING BETA-BUTYROLACTONE

A process for polymerizing β-butyrolactone is disclosed comprising contacting racemic β-butyrolactone or an enantiomer thereof with a catalyst/initiator system which comprises a rare earth metal, a chiral ligand, at least one nucleophilic ligand, optional

Design and synthesis of two-dimensional pillared MOF layers by connecting infinite one-dimensional chains via 4,4′-bipyridine

Two novel metal-organic frameworks, [Cd(Bna)(DMF)2(H 2O)2] n · nDMF (I) (Bna = 2,2′-dihydroxy-l,l′-dinaphthyl-3,3′-dicarboxylate) and [Cd(Bna)(Bipy)(DMF)2] n (II) (Bipy = 4,4′- bipyridine) have been synthesized under mild conditions and structurally characterized. Crystal structural analyses reveal that complex I adots a 1D spiral structure with DMF guest molecules in the spiral by hydrogen bondings. Complex II is constructed by -Cd-Bna-Cd- zigzag chains, which are further connected by Bipy into a 2D sheet. X-ray powder diffraction and thermogravimetric analyses for I and II show that they are highly themally stable in the solid state.

Chiral discrimination of α-amino acids with a C2-symmetric homoditopic receptor

Chiral discrimination of α-amino acids has been realized by a C 2-symmetric homoditopic receptor, which is based on a binaphthyl chiral skeleton with 2,2′diisopropoxy substituents and a common binding side arm, (o-carboxamido)-trifluoroacetophe