1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro-

Base Information

• Chemical Name: 1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro-
• CAS No.: 106824-80-0
• Molecular Formula: C₁₂H₁₁NO₂
• Molecular Weight: 201.225
• DSSTox Substance ID: DTXSID20147789
• Wikidata: Q83013178
• Mol file: 106824-80-0.mol

Synonyms:106824-80-0;5,6,7,8-tetrahydro-1H-benzo[f]indole-2,3-dione;1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro-;BRN 0158463;5,6,7,8-Tetrahydrobenz(f)isatin;5,6,7,8-Tetrahydro-1H-benz(f)indol-2,3-dione;DTXSID20147789;LS-33457

Chemical Property of 1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro-

Chemical Property:

• Density: 1.303 g/cm³
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 201.078978594
• Heavy Atom Count: 15
• Complexity: 313

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC2=CC3=C(C=C2C1)C(=O)C(=O)N3

Technology Process of 1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro-

There total 7 articles about 1H-Benz(f)indole-2,3-dione, 5,6,7,8-tetrahydro- 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:

hydroxyimino-acetic acid-(5,6,7,8-tetrahydro-[2]naphthylamide) (121186-56-9) → 5,6,7,8-Tetrahydrobenzisatin (106824-80-0)

Guidance literature:

With sulfuric acid; at 70 ℃;

Reference yield:

6-amino-1,2,3,4-tetrahydronaphthalene (2217-43-8) → 5,6,7,8-Tetrahydrobenzisatin (106824-80-0)

Guidance literature:

Multi-step reaction with 2 steps

1: diluted alcohol; hydroxylamine

2: sulfuric acid / 70 °C

With ethanol; sulfuric acid; hydroxylamine;

Reference yield:

(E)-5,6,7,8,5',6',7',8'-octahydro-1H,1'H-[2,2']bi[benz[f]indolylidene]-3,3'-dione → 5,6,7,8-Tetrahydrobenzisatin (106824-80-0)

Guidance literature:

With water; nitric acid; chromic acid;

upstream raw materials:

hydroxyimino-acetic acid-(5,6,7,8-tetrahydro-[2]naphthylamide)

7-nitro-3,4-dihydro-2H-naphthalen-1-one

6-amino-1,2,3,4-tetrahydronaphthalene

7-amino-1-tetralone

Downstream raw materials:

3-amino-5,6,7,8-tetrahydro-napthalene-2-carboxylic acid

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