34205-71-5

Basic information

• Product Name: 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester
• Synonyms: 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester;Methyl 4-hydroxynaphthalene-2-carboxylate;1-Hydroxy-naphthoesaeure-(3)-methylester;methyl 4-hydroxy-2-naphthoate
• CAS NO: 34205-71-5
• Molecular Formula: C₁₂H₁₀O₃
• Molecular Weight: 202.206
• Mol File: 34205-71-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 157-158 °C
• Boiling Point: 393.314°C at 760 mmHg
• Flash Point: 176.083°C
• Appearance: /
• Density: 1.265g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.642
• PKA: 8.63±0.40(Predicted)
• CAS DataBase Reference: 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester(34205-71-5)
• EPA Substance Registry System: 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester(34205-71-5)

Safety Data

• Hazardous Substances Data: 34205-71-5(Hazardous Substances Data)

Usage

General Description

2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester is a chemical compound that is the methyl ester of 4-hydroxy-2-naphthalenecarboxylic acid. It is a white crystalline solid with a molecular formula of C13H10O3 and a molecular weight of 214.21 g/mol. 2-Naphthalenecarboxylic acid, 4-hydroxy-, Methyl ester is commonly used in the production of pharmaceuticals, as well as in the synthesis of various organic compounds. It has been identified as a potential intermediate in the synthesis of biologically active compounds and is also used as a precursor in the production of fragrances and other specialty chemicals. Additionally, it has been studied for its potential antioxidant and anti-inflammatory properties.

InChI:InChI=1/C12H10O3/c1-15-12(14)9-6-8-4-2-3-5-10(8)11(13)7-9/h2-7,13H,1H3

Upstream product

• 127265-98-9 methyl 4-acetoxy-2-naphthoate 
• 67-56-1 methanol 
• 573-57-9 1,4-epoxy-1,4-dihydronaphthalene 
• 106-65-0 Dimethyl succinate 
• 100-52-7 benzaldehyde 
• 1573-91-7 3-hydroxynaphthoic acid 

Downstream Products

• 1572509-50-2 phenyl 4-hydroxy-2-naphthalenecarboxylate 

Relevant articles and documents

Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo[2.2.1]hept-2-ene synthones

The synthesis of SF5- and CF3-substituted benzenes and naphthalenes from various 7-oxanorbornene derivatives utilizing SF 5Cl and CF3I radical addition reactions, followed by dehydrohalogenation and aromatizatio

CYTOTOXIC AGENTS

The present invention provides a compound of formula (I): (T-X4)p-B1-X3-A-X2-L-X1-AM or pharmaceutically acceptable salts, tautomers, stereoisomers or mixtures thereof; wherein AM is (AM1); (AM2); or (AM3); with the proviso that the compound of formula (I) contains at least one sigma hole group; and with the proviso that no more than one of A, B1 and T is a sigma hole group; and each sigma hole group is independently: (SH1); (SH2); (SH3); (SH4); (SH5); (SH6); (SH7); (SH8); (SH9); or (SH10).

G-A CROSSLINKING CYTOTOXIC AGENTS

The invention relates to a compound of formula (I): or salts, solvates, isomers or tautomers thereof, wherein; A is a group selected from: R1 is selected from H and halogen; either R2 is selected from -CH2-halogen, C1