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1-(1-Naphtyl)-2-naphthol, with the molecular formula C20H14O, is a chemical compound featuring two naphthalene rings and a hydroxyl group attached to one of the rings. 1-(1-Naphtyl)-2-naphthol is recognized for its strong absorption and emission properties, making it a valuable asset in various scientific and medical applications.

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  • 73572-12-0 Structure
  • Basic information

    1. Product Name: 1-(1-Naphtyl)-2-naphthol
    2. Synonyms: 1-(1-Naphtyl)-2-naphthol;1,1'-Binaphthalen-2-ol
    3. CAS NO:73572-12-0
    4. Molecular Formula: C20H14O
    5. Molecular Weight: 270.32456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73572-12-0.mol
  • Chemical Properties

    1. Melting Point: 181-182.5 °C
    2. Boiling Point: 433.6±14.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1 +-.0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 8.91±0.50(Predicted)
    10. CAS DataBase Reference: 1-(1-Naphtyl)-2-naphthol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(1-Naphtyl)-2-naphthol(73572-12-0)
    12. EPA Substance Registry System: 1-(1-Naphtyl)-2-naphthol(73572-12-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 73572-12-0(Hazardous Substances Data)

73572-12-0 Usage

Uses

Used in Pharmaceutical and Biological Research:
1-(1-Naphtyl)-2-naphthol is used as a fluorescent dye for its strong absorption and emission properties, which are beneficial for fluorescence imaging and detection in biological and pharmaceutical research. Its ability to enhance the visualization of cellular structures and processes aids in advancing our understanding of biological systems and the development of new therapeutic strategies.
Used in Chemical Synthesis:
1-(1-Naphtyl)-2-naphthol serves as a key component in the synthesis of various organic compounds. Its unique structure and properties make it a versatile building block for creating a wide range of molecules with potential applications in different industries, including pharmaceuticals, materials science, and agrochemicals.
Used as a Reagent in Chemical Reactions:
1-(1-Naphtyl)-2-naphthol is also utilized as a reagent in chemical reactions, where it can participate in various processes such as oxidation, reduction, and substitution. Its reactivity and stability contribute to the development of new synthetic pathways and the production of novel compounds with specific properties and applications.
Used in Medical Research:
1-(1-Naphtyl)-2-naphthol has been studied for its potential antioxidant and anti-inflammatory properties, which could have significant implications in medical research. These properties may contribute to the development of new treatments for various diseases and conditions, including those involving oxidative stress and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 73572-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,7 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73572-12:
(7*7)+(6*3)+(5*5)+(4*7)+(3*2)+(2*1)+(1*2)=130
130 % 10 = 0
So 73572-12-0 is a valid CAS Registry Number.

73572-12-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-naphthalen-1-ylnaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names (R)-(+)-1,1'-binaphthol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73572-12-0 SDS

73572-12-0Relevant articles and documents

Steric effects of nucleophile-radical coupling reaction. Determination of rate constants for the reaction of aryl radicals with 2-naphthoxide anion

Tempesti, Tomas C.,Pierini, Adriana B.,Baumgartner, Maria T.

experimental part, p. 1523 - 1528 (2009/10/30)

The absolute rate constants for the reaction of different aryl radicals with 2-naphthoxide anion were determined using an indirect method, a competition of the coupling reaction with the H-atom abstraction. We here show that the radical-ambident nucleophi

PHOTOSTIMULATED REACTION OF ARYL IODIDES WITH 2-NAPHTHOXIDE IONS BY THE SRN1 MECHANISM

Pierini, A. B.,Baumgartner, M. T.,Rossi, R. A.

, p. 3429 - 3432 (2007/10/02)

The photostimulated reactions of p-iodoanisole (2) and 1-iodonaphthalene (7) with 2-naphthoxide ions in liquid ammonia gave the corresponding 1-aryl-2-naphthols as the only substitution product.These reactions are proposed to proceed via the SRN1 mechanism for nucleophilic aromatic substitution.

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