59866-97-6

Basic information

• Product Name: 5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER
• Synonyms: 5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER
• CAS NO: 59866-97-6
• Molecular Formula: C₁₂H₉BrO₂
• Molecular Weight: 265.11
• Mol File: 59866-97-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 268-274 °C(Press: 215 Torr)
• Appearance: /
• Density: 1.492±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER(59866-97-6)
• EPA Substance Registry System: 5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER(59866-97-6)

Safety Data

• Hazardous Substances Data: 59866-97-6(Hazardous Substances Data)

Usage

General Description

5-BROMO-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER is a chemical compound with the molecular formula C13H9BrO2. It is a methyl ester derivative of 5-bromo-1-naphthoic acid and is used in the synthesis of various organic compounds. This chemical is commonly utilized as a building block in the production of pharmaceuticals, dyes, and other fine chemicals. It is known for its high purity and high-quality properties, making it valuable in various chemical processes. Additionally, it is important to handle this compound with care due to its potential hazards, and proper safety measures should be followed when working with it.

Upstream product

• 16726-67-3 5-bromo-1-naphthalenecarboxylic acid 
• 77-78-1 dimethyl sulfate 
• 81-86-7 4-bromo-1,8-naphthalenedicarboxylic anhydride 
• 86-55-5 1-naphthalenecarboxylic acid 
• 67-56-1 methanol 
• 84532-82-1 5-bromo-1-naphthoyl chloride 

Downstream Products

• 91804-21-6 methyl 5-cyano-1-naphthylcarboxylate 
• 20366-57-8 (5-bromo-naphthalen-1-yl)-methanol 
• 42589-78-6 (+/-)-1.5-Dicarboxymethylacenaphthen 
• 4527-60-0 5-methyl-1-naphthoic acid 
• 20366-59-0 1-bromo-5-methylnaphthalene 
• 3839-20-1 5-cyanonaphthalene-1-carboxylic acid 
• 280135-08-2 5-(4-trifluoromethoxybenzyloxy)methyl-1-naphthaldehyde 
• 51934-37-3 5-methoxy-1-naphthoic acid 
• 865798-97-6 5-(2-amino-phenylsulfanyl)-naphthalene-1-carboxylic acid methyl ester 

Relevant articles and documents

Europium amphiphilic naphthalene based complex for the enhancement of linearly polarized luminescence in Langmuir-Blodgett films

Linearly polarized luminescence (LPL) in films of europium ions was induced by using naphthoic acid adopted alkyl chain (NaphC15), which plays the roles of both surfactant and photo-antenna. The synthesis of NaphC15 was newly developed, and the Eu complex composed in a 1:3 ratio of Eu3+ ion and NaphC15 was synthesized in the powder form for comparison. The structural aspects of LB films with a layered scheme were obtained from the measurements of synchrotron XRPD, X-ray photoelectron spectroscopy and waveguide polarized absorption spectra. Luminescence of europium in the film is more intense than that in the powdered complex. The luminescence efficiency calculated from the observed luminescence lifetimes and quantum yields also supported their structure-enhanced luminescence. Finally, we revealed that the LPL was sensitized by the electronic dipole moment localized on the NaphC15 moieties aligned independently in the Langmuir-Blodgett films.

COMPOUNDS FOR BINDING PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9 (PCSK9)

The present disclosure relates to novel compounds, methods, and compositions capable of binding to PCSK9, thereby modulating PCSK9 proprotein convertase enzyme activity. The compounds of the disclosure include compounds Formula (I).

Synthesis, antitumor and DNA photocleaving activities of novel naphthalene carboxamides: Effects of different thio-heterocyclic rings and aminoalkyl side chains

Two kinds of thio-heterocyclic fused naphthalene carboxamides, 3a-b, 4a-b, were designed, synthesized and quantitatively evaluated as efficient antitumor and DNA photocleaving agents. Compound 3a or 3b, having the thiophene ring, intercalated into DNA mor