14461-81-5

Basic information

• Product Name: 3-propylnaphthalen-2-ol
• Synonyms: 2-Naphthol, 3-propyl-; 3-Propyl-2-naphthol
• CAS NO: 14461-81-5
• Molecular Formula: C₁₃H₁₄O
• Molecular Weight: 186.2497
• Mol File: 14461-81-5.mol

Chemical Properties

• Boiling Point: 327.2°C at 760 mmHg
• Flash Point: 156.7°C
• Density: 1.087g/cm³
• Vapor Pressure: 0.000108mmHg at 25°C
• Refractive Index: 1.619
• CAS DataBase Reference: 3-propylnaphthalen-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-propylnaphthalen-2-ol(14461-81-5)
• EPA Substance Registry System: 3-propylnaphthalen-2-ol(14461-81-5)

Safety Data

• Hazardous Substances Data: 14461-81-5(Hazardous Substances Data)

Upstream product

• 93-04-9 2-Methoxynaphthalene 
• 852281-24-4 1-(o-ethynylphenyl)-pent-1-ene 
• 68251-77-4 2‐bromo‐3‐methoxynaphthalene 
• 920-39-8 isopropylmagnesium bromide 

Downstream Products

• 118683-54-8 3-Methoxy-4-(3-propyl-naphthalen-2-yloxymethyl)-benzoic acid 

Relevant articles and documents

ORGANIC COMPOUND, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

An organic compound has a benzonaphthofuran skeleton and is represented by Formula (G1). In Formula (G1), A represents a pyrene skeleton. In the case where the pyrene skeleton has a substituent, the substituent is a diarylamino group including two substituted or unsubstituted aryl groups each having 6 to 13 carbon atoms, a substituted or unsubstituted aryl group having 6 to 13 carbon atoms, an alkyl group having 1 to 7 carbon atoms, a substituted or unsubstituted monocyclic saturated hydrocarbon group having 3 to 20 carbon atoms, or a substituted or unsubstituted poly cyclic saturated hydrocarbon group having 7 to 10 carbon atoms. The two aryl groups of the diarylamino group may be the same or different. In X1 represented by Formula (G1-1), one of R6 and R7 is bonded to N in Formula (G1), and the other of R6 and R7 represents an alkyl group having 1 to 7 carbon atoms, a substituted or unsubstituted monocyclic saturated hydrocarbon group having 3 to 20 carbon atoms, or a substituted or unsubstituted poly cyclic saturated hydrocarbon group having 7 to 10 carbon atoms.

De Novo Synthesis of Phenols and Naphthols through Oxidative Cycloaromatization of Dienynes

In this work, a rhodium-catalyzed oxidative cycloaromatization of dienynes, which provides a highly straightforward and efficient way to access polysubstituted naphthols and phenols under mild conditions, is described. Challenged electron-withdrawing groups are well tolerated in this protocol, and late-stage phenyl ring formation is demonstrated.

Ruthenium-catalyzed cyclization of epoxide with a tethered alkyne: Formation of ketene intermediates via oxygen transfer from epoxides to terminal alkynes

Treatment of (o-ethynyl)phenyl epoxides with TpRuPPh3(CH 3CN)2PF6 (10 mol %) in hot toluene (100 °C, 3-6 h) gave 2-naphthols or 1-alkylidene-2-indanones very selectively with isolated yields exceeding 72%, depen