2-Benzylidene-3-oxo-5-indanacetic acid

Base Information

Chemical Name:2-Benzylidene-3-oxo-5-indanacetic acid
CAS No.:71823-58-0
Molecular Formula:C18H14O3
Molecular Weight:278.307
Hs Code.:

Synonyms:BRN 2988212;2-Benzylidene-3-oxo-5-indanacetic acid;5-Indanacetic acid, 2-benzylidene-3-oxo-;71823-58-0;LS-81030

Suppliers and Price of 2-Benzylidene-3-oxo-5-indanacetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-Benzylidene-3-oxo-5-indanacetic acid

Chemical Property:

Vapor Pressure:7.72E-12mmHg at 25°C
Boiling Point:524.7°Cat760mmHg
Flash Point:285.2°C
Density:1.323g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:278.094294304
Heavy Atom Count:21
Complexity:445

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2=C(C=C(C=C2)CC(=O)O)C(=O)C1=CC3=CC=CC=C3
Isomeric SMILES:C\1C2=C(C=C(C=C2)CC(=O)O)C(=O)/C1=C\C3=CC=CC=C3

Technology Process of 2-Benzylidene-3-oxo-5-indanacetic acid

There total 2 articles about 2-Benzylidene-3-oxo-5-indanacetic 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:

: 39105-51-6
3-(4-acetylphenyl)propionic acid

: 71823-58-0
{3-Oxo-2-[1-phenyl-meth-(Z)-ylidene]-indan-5-yl}-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: (i) Mor, sulfur, (ii) aq. NaOH, EtOH

2: polyphosphoric acid

3: aq. KOH / ethanol

With potassium hydroxide; PPA; In ethanol;
DOI:10.1021/jm00198a007