701270-26-0

Basic information

• Product Name: 2-butyl-6-Methoxy-naphthalene
• Synonyms: 2-butyl-6-Methoxy-naphthalene
• CAS NO: 701270-26-0
• Molecular Formula: C₁₅H₁₈O
• Molecular Weight: 214.30282
• Product Categories: Aliphatics, Aromatics, Impurities
• Mol File: 701270-26-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Ethyl Acetate
• CAS DataBase Reference: 2-butyl-6-Methoxy-naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-butyl-6-Methoxy-naphthalene(701270-26-0)
• EPA Substance Registry System: 2-butyl-6-Methoxy-naphthalene(701270-26-0)

Safety Data

• Hazardous Substances Data: 701270-26-0(Hazardous Substances Data)

Usage

Description

2-butyl-6-Methoxy-naphthalene is an organic compound with the chemical formula C15H18O. It is characterized by the presence of a naphthalene ring, a butyl group attached to the second carbon, and a methoxy group attached to the sixth carbon. 2-butyl-6-Methoxy-naphthalene is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
2-butyl-6-Methoxy-naphthalene is used as an impurity in Nabumetone (N200500), which is an anti-inflammatory and antibacterial agent. Its presence in Nabumetone may affect the drug's efficacy and safety, making it important to monitor and control its levels during the manufacturing process.

Upstream product

• 4426-47-5 butylboronic acid 
• 5111-65-9 2-Bromo-6-methoxynaphthalene 
• 100975-88-0 1-(6-methoxynaphth-2-yl)butan-1-one 
• 93-04-9 2-Methoxynaphthalene 
• 1416330-91-0 C₁₃H₁₅NO₄S 
• 693-04-9 butyl magnesium bromide 
• 693-03-8 n-butyl magnesium bromide 
• 109-72-8 n-butyllithium 
• 67886-68-4 6-chloro-2-methoxynaphthalene 

Relevant articles and documents

Nestable Tetrakis(spiroborate) Nanocycles

Multicomponent construction of the tetrakis(spiroborate) anionic nanocycles was achieved by reacting bis(dihydroxynaphthalene)s with tetrahydroxyanthraquinone in the presence of boric acid in a self-organized manner. These nanocycles exhibited selective molecular recognition behavior toward cationic guests such as methyl viologen derivatives. Formation of a supramolecular ring@ring and a guest@ring@ring structure was observed by combining the anionic nanocycle and the vinylogous analog of cyclobis(paraquat-p-phenylene). (Figure Presented).

Iron-catalyzed cross-coupling reactions of alkyl grignards with aryl sulfamates and tosylates

The iron-catalyzed cross-coupling of aryl sulfamates and tosylates has been achieved with primary and secondary alkyl Grignards. This study of iron-catalyzed cross-coupling reactions also examines the isomerization and β-hydride elimination problems that are associated with the use of isopropyl nucleophiles. While a variety of iron sources were competent in the reaction, the use of FeF3·3H2O was critical to minimize nucleophile isomerization.

Synthesis and characterization of liquid crystalline semiconducting materials, dialkyl-2-phenylnaphthalene derivatives - Mesomorphic behavior and charge carrier transport

For establishment of high electronic change carrier transport at ambient temperature, dialkyl derivatives of 2-phenylnaphthalene have been synthesized and characterized their liquid crystalline behaviors and photoelectrical properties. These materials exhibited smectic masophases (Smectic A, B and E phases), at fairly low temperature range extended down below ambient temperature. Fast electronic transport of positive carriers was observed in SmE phase, of 2-(4′-octylphenyl)-6-butylnaphthalene at 30°C, whose mobility was over 10-2 cm2/Vs.