1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester

Base Information

• Chemical Name: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester
• CAS No.: 573674-19-8
• Molecular Formula: C₁₇H₁₂O₃
• Molecular Weight: 264.28
• DSSTox Substance ID: DTXSID60699772
• Nikkaji Number: J1.919.073K
• Wikidata: Q82630799
• Mol file: 573674-19-8.mol

Synonyms:573674-19-8;1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester;(4-hydroxyphenyl) naphthalene-1-carboxylate;4-Hydroxyphenyl 1-naphthoate;1-Naphthalenecarboxylic acid,4-hydroxyphenyl ester;4-Hydroxyphenyl ester1-naphthalenecarboxylic acid;4-Hydroxyphenyl1-naphthoate;DTXSID60699772;4-HYDROXYPHENYL NAPHTHALENE-1-CARBOXYLATE;Naphthalene-1-carboxylic acid 4-hydroxyphenyl ester

Chemical Property of 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester

Chemical Property:

• Vapor Pressure: 1.68E-09mmHg at 25°C
• Boiling Point: 471.2°C at 760 mmHg
• Flash Point: 203.9°C
• PSA: 46.53000
• Density: 1.286g/cm³
• LogP: 3.76460
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 264.078644241
• Heavy Atom Count: 20
• Complexity: 333

Purity/Quality:

98% ^*data from raw suppliers

4-HYDROXYPHENYL ESTER 1-NAPHTHALENECARBOXYLIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C=CC=C2C(=O)OC3=CC=C(C=C3)O

Technology Process of 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester

There total 1 articles about 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 36.0%

hydroquinone (123-31-9,8027-02-9) + naphthalene-1-carbonic acid chloride (879-18-5) → 4-hydroxyphenyl 1-naphthoate (573674-19-8)

Guidance literature:

In diethyl ether; at 20 ℃; for 1h;

DOI:10.1016/S0040-4020(03)00737-3

upstream raw materials:

hydroquinone

naphthalene-1-carbonic acid chloride