1,8-Dibenzoylnaphthalene

Base Information

• Chemical Name: 1,8-Dibenzoylnaphthalene
• CAS No.: 19274-72-7
• Molecular Formula: C24H16 O2
• Molecular Weight: 336.39
• Hs Code.: 2914399090
• European Community (EC) Number: 242-929-6
• NSC Number: 97756
• UNII: 6JF9JBM8WX
• DSSTox Substance ID: DTXSID8066474
• Nikkaji Number: J242.756G
• Wikidata: Q81993055
• Mol file: 19274-72-7.mol

Synonyms:1,8-Dibenzoylnaphthalene;19274-72-7;Naphthalene, 1,8-dibenzoyl-;(8-benzoylnaphthalen-1-yl)-phenylmethanone;6JF9JBM8WX;Methanone, 1,8-naphthalenediylbis(phenyl-;Methanone, 1,8-naphthalenediylbis[phenyl-;EINECS 242-929-6;NSC 97756;NSC-97756;Methanone, 1,1'-(1,8-naphthalenediyl)bis(1-phenyl-;NSC97756;1.8-Dibenzoylnaphthalin;Naphthalene,8-dibenzoyl-;UNII-6JF9JBM8WX;(8-benzoylnaphthalen-1-yl)(phenyl)methanone;DTXSID8066474;AKOS024338089;Methanone,8-naphthalenediylbis[phenyl-;Naphthalene-1,8-diylbis(phenylmethanone);1,1'-(1,8-NAPHTHALENEDIYL)BIS(1-PHENYLMETHANONE)

Chemical Property of 1,8-Dibenzoylnaphthalene

Chemical Property:

• Vapor Pressure: 2.06E-11mmHg at 25°C
• Boiling Point: 532.3°Cat760mmHg
• Flash Point: 195.8°C
• PSA: 34.14000
• Density: 1.202g/cm³
• LogP: 5.30180
• XLogP3: 5.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 336.115029749
• Heavy Atom Count: 26
• Complexity: 454

Purity/Quality:

98%,99%, ^*data from raw suppliers

1,8-DIBENZOYLNAPHTHALENE AldrichCPR ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)C2=CC=CC3=C2C(=CC=C3)C(=O)C4=CC=CC=C4

Technology Process of 1,8-Dibenzoylnaphthalene

There total 26 articles about 1,8-Dibenzoylnaphthalene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,2-diphenyl-acenaphthylene (13638-84-1) → 1,8-dibenzoylnaphthalene (19274-72-7)

Guidance literature:

With chromium(VI) oxide; acetic acid;

DOI:10.1021/ja01290a024

Reference yield:

cis-diphenylacenaphthylenediol (58335-01-6) → 1,8-dibenzoylnaphthalene (19274-72-7)

Guidance literature:

With lead(IV) acetate; acetic acid;

DOI:10.1021/ja01230a044

Reference yield:

phenylmagnesium bromide → 1,8-dibenzoylnaphthalene (19274-72-7)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether; benzene / Kochen des nach der Hydrolyse erhaltenen Reaktionsprodukts mit H₂SO₄ in Eisessig

2: CrO₃; acetic acid

With chromium(VI) oxide; diethyl ether; acetic acid; benzene;

DOI:10.1021/ja01290a024

upstream raw materials:

Perbenzoic acid

chloroform

1,2-diphenyl-acenaphthylene

cis-diphenylacenaphthylenediol

Downstream raw materials:

cis-diphenylacenaphthylenediol

1,3-diphenyl-1H,3H-benz[de]isochromene

1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol

1,2-diphenyl-acenaphthylene