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1,5-Dibenzoylnaphthalene is a chemical compound derived from naphthalene, featuring two benzoyl groups attached to the 1 and 5 positions of the naphthalene ring. It is recognized for its versatility in organic chemistry due to its ability to participate in various chemical reactions, such as Friedel-Crafts acylation and nucleophilic substitution. This makes it a valuable building block in the synthesis of dyes, pigments, and other organic compounds.

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  • 83-80-7 Structure
  • Basic information

    1. Product Name: 1,5-DIBENZOYLNAPHTHALENE
    2. Synonyms: 1,5-Naphthalenediylbis(phenylmethanone);5-Benzoyl-1-naphtyl(phenyl) ketone;[5-(benzoyl)-1-naphthyl]-phenyl-methanone;[5-(benzoyl)naphthalen-1-yl]-phenylmethanone;phenyl-(5-phenylcarbonylnaphthalen-1-yl)methanone;Methanone, 1,5-naphthalenediylbis[phenyl-;1,5-DIBENZOYLNAPHTHALENE;1,5-dibenzoyl-2-naphthaene
    3. CAS NO:83-80-7
    4. Molecular Formula: C24H16O2
    5. Molecular Weight: 336.38
    6. EINECS: 201-502-4
    7. Product Categories: N/A
    8. Mol File: 83-80-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 532.3 °C at 760 mmHg
    3. Flash Point: 195.8 °C
    4. Appearance: /
    5. Density: 1.202 g/cm3
    6. Vapor Pressure: 2.06E-11mmHg at 25°C
    7. Refractive Index: 1.663
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,5-DIBENZOYLNAPHTHALENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,5-DIBENZOYLNAPHTHALENE(83-80-7)
    12. EPA Substance Registry System: 1,5-DIBENZOYLNAPHTHALENE(83-80-7)
  • 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: 83-80-7(Hazardous Substances Data)

83-80-7 Usage

Uses

Used in Organic Synthesis:
1,5-Dibenzoylnaphthalene is used as a reagent in organic synthesis for its capacity to undergo multiple chemical reactions, contributing to the creation of a wide range of organic compounds.
Used in Dye and Pigment Production:
As a starting material, 1,5-dibenzoylnaphthalene is utilized in the production of dyes and pigments, given its chemical properties that facilitate the development of colorants for various applications.
Used in Research and Pharmaceutical Industries:
1,5-Dibenzoylnaphthalene is employed in research and pharmaceutical industries as a starting material for the synthesis of new pharmaceutical compounds and other functional materials, owing to its reactivity and structural features that can be manipulated for specific purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 83-80-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83-80:
(4*8)+(3*3)+(2*8)+(1*0)=57
57 % 10 = 7
So 83-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H16O2/c25-23(17-9-3-1-4-10-17)21-15-7-14-20-19(21)13-8-16-22(20)24(26)18-11-5-2-6-12-18/h1-16H

83-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-benzoylnaphthalen-1-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names (5-benzoylnaphthalen-1-yl)(phenyl)methanone

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:83-80-7 SDS

83-80-7Relevant articles and documents

Incorporation of the 1,5-naphthalene subunit into heteroporphyrin structure: Toward helical aceneporphyrinoids

Szyszko, Bartosz,Pacholska-Dudziak, Ewa,Latos-Grazyński, Lechos?aw

, p. 5090 - 5095 (2013)

5,10,15,20-Tetraaryl-22-hetero-1,5-naphthiporphyrins, which contain a 1,5-naphthylene moiety instead of one pyrrole embedded in the macrocyclic framework of heteroporphyrins, were obtained by the [3 + 1] approach using the 1,5-naphthylene analogue of tripyrrane (1,5-bis(phenyl(2-pyrolyl)methyl) naphthalene) and 2,5-bis(arylhydroxymethyl)heterocyclopentadiene (heterocyclopentadiene: thiophene, selenophene, tellurophene). The steric constraints, imposed by the substitution mode of the 1,5-naphthylene building block, resulted in the specific helical conformation of 22-hetero-1,5- naphthiporphyrins. The spectroscopic and structural properties of these aceneporphyrinoids indicate a lack of macrocycle aromaticity. Their protonation yielded solely dicationic species.

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