67886-69-5

Basic information

• Product Name: Naphthalene, 2-iodo-6-methoxy- (9CI)
• Synonyms: Naphthalene, 2-iodo-6-methoxy- (9CI)
• CAS NO: 67886-69-5
• Molecular Formula: C₁₁H₉IO
• Molecular Weight: 284.09303
• Product Categories: NAPHTALENE
• Mol File: 67886-69-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 347.7°Cat760mmHg
• Flash Point: 164.1°C
• Appearance: /
• Density: 1.674g/cm³
• Vapor Pressure: 0.000106mmHg at 25°C
• Refractive Index: 1.674
• CAS DataBase Reference: Naphthalene, 2-iodo-6-methoxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 2-iodo-6-methoxy- (9CI)(67886-69-5)
• EPA Substance Registry System: Naphthalene, 2-iodo-6-methoxy- (9CI)(67886-69-5)

Safety Data

• Hazardous Substances Data: 67886-69-5(Hazardous Substances Data)

Usage

General Description

2-Iodo-6-methoxy-naphthalene is a chemical compound with the molecular formula C11H9IO. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon. 2-Iodo-6-methoxy-naphthalene is used in organic synthesis and pharmaceutical research as a building block for the preparation of various compounds. It is primarily utilized in the synthesis of biologically active molecules and pharmaceutical intermediates. This chemical has potential applications in the development of new drugs and therapeutic agents. Additionally, it may also be used as a reference standard for analytical testing and research purposes.

InChI:InChI=1/C11H9IO/c1-13-11-5-3-8-6-10(12)4-2-9(8)7-11/h2-7H,1H3

Upstream product

• 32721-21-4 1-iodo-2-methoxynapthalene 
• 109-72-8 n-butyllithium 
• 5111-65-9 2-Bromo-6-methoxynaphthalene 
• 93-04-9 2-Methoxynaphthalene 
• 7732-18-5 water 

Downstream Products

• 93-04-9 2-Methoxynaphthalene 
• 1378521-72-2 C₁₉H₁₈O 
• 1278587-56-6 C₂₂H₁₉⁽²⁾HN₂O₂ 
• 1278587-54-4 1-methyl-2-(4-methoxyphenyl)-5-(6-methoxy-2-naphthyl)-1H-imidazole 
• 1278587-57-7 1-methyl-2-(4-methanesulfinyl-2-methylphenyl)-5-(6-methoxynaphthalen-2-yl)-1H-imidazole 
• 1278587-40-8 1-methyl-2-(2-methoxyphenyl)-5-(6-methoxy-2-naphthyl)-1H-imidazole 
• 1278587-39-5 1-methyl-2-(2-methylphenyl)-5-(6-methoxy-2-naphthyl)-1H-imidazole 
• 1278587-36-2 1-methyl-2-(4-fluorophenyl)-5-(6-methoxy-2-naphthyl)-1H-imidazole 
• 1278587-35-1 1-methyl-2-(4-trifluoromethylphenyl)-5-(6-methoxy-2-naphthyl)-1H-imidazole 
• 956613-00-6 1-methyl-2-(4-methanesulfinyl-2-methylphenyl)-4-(4-pyridyl)-5-(6-methoxynaphthalen-2-yl)-1H-imidazole 
• 27602-75-1 2-(6-methoxy-2-naphthyl)propanal 
• 194606-21-8 Acetic acid (S)-2-(6-methoxy-naphthalen-2-yl)-3-(toluene-4-sulfonyloxy)-propyl ester 

Relevant articles and documents

N6-arylation of 2′-deoxyadenosine via copper-catalyzed direct coupling with aryl halides

(Chemical Equation Presented) A general method for efficient N 6-arylation of 2′-deoxyadenosine via copper-catalyzed direct coupling with aryl iodides and bromides is described. The method is useful for aryl halides with either electron-donatin

REACTIVE MESOGENIC COMPOUNDS AND MIXTURES

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Lipase-mediated asymmetric construction of 2-arylpropionic acids: Enantiocontrolled syntheses of S-naproxen and S-ibuprofen

A general and enantiocontrolled synthetic route to 2-arylpropionic acids, represented by non-steroidal anti-inflammatory drugs S-naproxen 1a and S-ibuprofen 1b, has been developed by employing the lipase-mediated asymmetric acetylation of prochiral 2-aryl-1,3-propanediol 3, which has been derived via a Heck reaction, as the key step.