61982-91-0

Basic information

• Product Name: 5-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHOL
• Synonyms: 5-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHOL
• CAS NO: 61982-91-0
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Mol File: 61982-91-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 324.4°C at 760 mmHg
• Flash Point: 149.4°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 0.000101mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: 5-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHOL(61982-91-0)
• EPA Substance Registry System: 5-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHOL(61982-91-0)

Safety Data

• Hazardous Substances Data: 61982-91-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H14O2/c1-13-11-7-3-4-8-9(11)5-2-6-10(8)12/h3-4,7,10,12H,2,5-6H2,1H3

Upstream product

• 40771-26-4 1,2,3,4-tetrahydro-1,5-dihydroxy-naphthalene 
• 138-24-9 phenyltrimethylammonium chloride 
• 33892-75-0 5-Methoxy-1-tetralone 
• 5123-13-7 5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane 

Downstream Products

• 60573-59-3 8-Methoxy-1,2-dihydronaphthalene 
• 132449-38-8 1-chloro-5-methoxy-1,2,3,4-tetrahydronaphthalene 
• 690232-04-3 1-benzyl-5-methoxy-1,2,3,4-tetrahydronaphthalene 
• 40771-26-4 1,2,3,4-tetrahydro-1,5-dihydroxy-naphthalene 
• 41552-07-2 1-oxo-5-hydroxy-6-methyl-1,2,3,4-tetrahydronaphthalene 
• 1041185-08-3 4,10-dimethoxy-1,2,3,6b,7,8,9,12b-octahydroperylene 
• 1041185-11-8 4,10-dimethoxy-1,2,3,7,8,9-hexahydroperylene 
• 1008-19-1 5-methoxy-1,2,3,4-tetrahydro-naphthalene 
• 33892-75-0 5-Methoxy-1-tetralone 
• 200425-71-4 (-)-(R)-5-Methoxy-1-tetralol 
• 182497-75-2 (+)-(S)-5-Methoxy-1-tetralol 
• 1292823-26-7 1-benzoyloxy-5-methoxytetralin 
• 41566-70-5 1-amino-5-methoxy-1,2,3,4-tetrahydronaphthalene hydrochloride 

Relevant articles and documents

A nickel catalyst for the addition of organoboronate esters to ketones and aldehydes

A Ni(cod)2/IPr catalyst promotes the intermolecular 1,2-addition of arylboronate esters to unactivated aldehydes and ketones. Dlaryl, alkyl aryl, and dialkyl ketones show good reactivity under mild reaction conditions (3) with aryl ether substrates. A Ni(0)/Ni(II) catalytic cycle initiated by the oxidative cyclization of the carbonyl substrate Is proposed.