57944-44-2

Basic information

• Product Name: 2-Naphthalenol,7-ethoxy-(9CI)
• Synonyms: 7-ethoxynaphthalen-2-ol;7-Ethoxy-2-naphthol;2-Naphthalenol,7-ethoxy-(9CI);7-Ethoxy-2-naphthalenol;2-Naphthalenol, 7-ethoxy
• CAS NO: 57944-44-2
• Molecular Formula: C₁₂H₁₂O₂
• Molecular Weight: 188.23
• Product Categories: NAPHTALENE;API intermediates
• Mol File: 57944-44-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 347.5 °C at 760 mmHg
• Flash Point: 209.8 °C
• Appearance: /
• Density: 1.158
• Vapor Pressure: 2.68E-05mmHg at 25°C
• Refractive Index: 1.622
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 9.47±0.40(Predicted)
• CAS DataBase Reference: 2-Naphthalenol,7-ethoxy-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenol,7-ethoxy-(9CI)(57944-44-2)
• EPA Substance Registry System: 2-Naphthalenol,7-ethoxy-(9CI)(57944-44-2)

Safety Data

• Hazardous Substances Data: 57944-44-2(Hazardous Substances Data)

Usage

General Description

2-Naphthalenol,7-ethoxy-(9CI) is a specific type of compound that belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings. Specific information about this chemical, such as its physical and chemical properties, toxicity, and potential uses, is not widely available in the public domain. As with any kind of chemical compounds, it's crucial to handle 2-Naphthalenol,7-ethoxy-(9CI) properly and observe proper safety measures, given the potential risks and hazards involving chemical handling and exposure. It's recommended to consult scientific resources or professionals for comprehensive and specific details about this compound.

InChI:InChI=1/C12H12O2/c1-2-14-12-6-4-9-3-5-11(13)7-10(9)8-12/h3-8,13H,2H2,1H3

Upstream product

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Relevant articles and documents

Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-Quinones: Platform Molecules for Diversity-Oriented Synthesis of Biaryldiols

Presented here is a class of novel axially chiral aryl-p-quinones as platform molecules for the preparation of non-C2 symmetric biaryldiols. Two sets of aryl-p-quinone frameworks were synthesized with remarkable enantiocontrol by means of chiral phosphoric acid catalyzed enantioselective arylation of p-quinones by central-to-axial chirality conversion. These aryl-p-quinones were then used to access a wide spectrum of highly functionalized non-C2 symmetric biaryldiols with excellent retention of the enantiopurity.