15442-73-6

Basic information

• Product Name: Diethyl-2,6-naphthalenedicarboxylate
• Synonyms: Diethyl-2,6-naphthalenedicarboxylate;diethyl naphthalene-2,6-dicarboxylate;2,6-Naphthalenedicarboxylicacid, 2,6-diethyl ester
• CAS NO: 15442-73-6
• Molecular Formula: C16H14O4-2
• Molecular Weight: 270.27996
• Mol File: 15442-73-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 121-126 °C
• Boiling Point: 400.323°C at 760 mmHg
• Flash Point: 199.726°C
• Appearance: /
• Density: 1.172g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.576
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Diethyl-2,6-naphthalenedicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Diethyl-2,6-naphthalenedicarboxylate(15442-73-6)
• EPA Substance Registry System: Diethyl-2,6-naphthalenedicarboxylate(15442-73-6)

Safety Data

• Hazardous Substances Data: 15442-73-6(Hazardous Substances Data)

Usage

General Description

Diethyl-2,6-naphthalenedicarboxylate, also known as 2,6-Naphthalenedicarboxylic acid diethyl ester, is a chemical compound that is commonly used as a raw material in the synthesis of pharmaceuticals and agrochemicals. It is a white to off-white crystalline powder with a molecular formula of C16H14O4 and a molecular weight of 270.28 g/mol. Diethyl-2,6-naphthalenedicarboxylate is soluble in most organic solvents and is stable under normal conditions of use and storage. Diethyl-2,6-naphthalenedicarboxylate is commonly employed as an intermediate in the production of dyes, pigments, and other specialty chemicals due to its unique molecular structure and reactivity. It is important to handle and store this chemical with appropriate safety precautions due to its potential flammability and irritant properties.

InChI:InChI=1/C16H16O4/c1-3-19-15(17)13-7-5-12-10-14(16(18)20-4-2)8-6-11(12)9-13/h5-10H,3-4H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 840-65-3 dimethyl 2,6-naphthalenedicarboxylate 
• 1141-38-4 2,6-Naphthalenedicarboxylic acid 

Downstream Products

• 959282-81-6 naphthalene-2,6-dicarboxylic acid monoethyl ester 

Relevant articles and documents

Self-assembly of porphyrin-azulene-porphyrin and porphyrin-azulene conjugates

In this paper we report the synthesis and self-assembling behavior of new porphyrin-azulene-porphyrin and porphyrin-azulene conjugates. The porphyrin-azulene-porphyrin conjugate gelates a number of organic solvents, while the porphyrin-azulene conjugates form vesicles in a chloroform-methanol binary mixture. The structures of the organogels and vesicles have been characterized by SEM and AFM. Two porphyrin-naphthalene-porphyrin and porphyrin-naphthalene conjugates were also prepared. A comparison of their properties with those of the azulene analogues reveals that the intermolecular dipole-dipole interaction of the azulene units plays an important role in promoting the self-assembly of the porphyrin-azulene-porphyrin and porphyrin-azulene conjugates. The Royal Society of Chemistry 2009.

Quaternary ammonium compounds having muscle relaxation activity

A quaternary ammonium having a muscle relaxation activity compound represented by the formula (I): STR1 wherein R1 represents a methylene, a lower alkylenoxy, a lower alkenylene, a lower alkynylene, --CO--, --COO--, a lower alkylene carbonyloxy, --CH(OR5)--, a lower alkylenecarbonyl, a hydroxy lower alkylene, --O--, --S--, --SO--, or --SO2 --; R2 represents a hydrogen atom, a hydroxy lower alkyl, an aldehyde, a lower alkyl carbonyl, --NO2, or --NHR6 ; R3 represents a hydrogen atom of a group --R1 --(CH2)a --[CH(CH2 A)--CH2 ]b --A; R4 represents an anion; R5 and R6 represent a hydrogen atom or a acetyl; A represents a quaternary ammonium group; a represents an integer of 1 to 8; b represents 0 or 1; m represents an integer of 1 to 4; and (Z) represents a trivalent benzene ring, a trivalent naphthalene ring, a trivalent diphenyl or a trivalent ethane radical.