2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid

Base Information

• Chemical Name: 2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid
• CAS No.: 61959-33-9
• Molecular Formula: C18H16O3
• Molecular Weight: 280.323
• DSSTox Substance ID: DTXSID90402958
• Wikidata: Q82206486

Synonyms:2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid;61959-33-9;ST50981083;Oprea1_598317;SCHEMBL12877794;DTXSID90402958;HVCVQWLJNZXBHT-UHFFFAOYSA-N;Benzoic acid, 2-[(5,6,7,8-tetrahydro-2-naphthalenyl)carbonyl]-;AKOS009236481;2-(5,6,7,8-tetrahydronaphthalen-2-ylcarbonyl)benzoic acid

Chemical Property of 2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid

Chemical Property:

• XLogP3: 4.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 280.109944368
• Heavy Atom Count: 21
• Complexity: 403

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC2=C(C1)C=CC(=C2)C(=O)C3=CC=CC=C3C(=O)O

Technology Process of 2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid

There total 2 articles about 2-(5,6,7,8-tetrahydronaphthalene-2-carbonyl)benzoic Acid 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: 93.0%

phthalic anhydride (85-44-9) + tetralin (119-64-2) → 5-(o-carboxybenzoyl)-1,2,3,4-tetrahydronaphthalene (61959-33-9)

Guidance literature:

With aluminum (III) chloride; In neat (no solvent); for 1h; Milling;

DOI:10.3762/bjoc.15.130

Reference yield:

phthalic anhydride (85-44-9) + aluminium trichloride (7446-70-0) + tetralin (119-64-2) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → 5-(o-carboxybenzoyl)-1,2,3,4-tetrahydronaphthalene (61959-33-9)

Guidance literature:

at 60 - 70 ℃;

Reference yield: 66.3%

5-(o-carboxybenzoyl)-1,2,3,4-tetrahydronaphthalene (61959-33-9) + 4-(methylsulfonyl)phenylhydrazine (877-66-7) → 2-(4-methanesulfonylphenyl)-4-(5,6,7,8-tetrahydronaphthalen-2-yl)phthalazin-1-one

Guidance literature:

In ethanol; Reflux;

DOI:10.1002/ardp.201500336

upstream raw materials:

phthalic anhydride

tetralin

aluminium trichloride

benzene

Downstream raw materials:

1,2,3,4-tetrahydronaphthacene-6,11-quinone

1,2,3,4-tetrahydrobenzanthracene-7,12-dione

2-(5,6,7,8-tetrahydro-[2]naphthylmethyl)-benzoic acid

5,12-dihydro-naphthacene

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