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Technology Process of 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-

1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-

Base Information
  • Chemical Name:1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-
  • CAS No.:6396-90-3
  • Molecular Formula:C19H11 N O5
  • Molecular Weight:333.29434
  • Hs Code.:
  • European Community (EC) Number:229-006-3,241-731-7
  • DSSTox Substance ID:DTXSID3064306,DTXSID4066254
  • Nikkaji Number:J207.004I,J106.043K,J3.573.843F
  • Wikidata:Q81991432
  • Mol file:6396-90-3.mol
1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-

Synonyms:6396-90-3;17739-41-2;1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-;2-(3-Hydroxy-2(1H)-quinolylidene)-1,3-dioxoindan-5-carboxylic acid;1H-Indene-6-carboxylic acid, 3-hydroxy-2-(3-hydroxy-2-quinolinyl)-1-oxo-;3-Hydroxy-2-(3-hydroxy-2-quinolyl)-1-oxo-1H-indene-6-carboxylic acid;EINECS 229-006-3;EINECS 241-731-7;DTXSID3064306;DTXSID4066254;SCHEMBL13929116;3-Hydroxy-2-(3-hydroxy-2-quinolinyl)-1-oxo-1H-indene-6-carboxylic acid

Suppliers and Price of 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 5 raw suppliers
Chemical Property of 1H-Indene-5-carboxylic acid, 2,3-dihydro-2-(3-hydroxy-2(1H)-quinolinylidene)-1,3-dioxo-
Chemical Property:
  • Vapor Pressure:1.21E-12mmHg at 25°C 
  • Boiling Point:543.5°C at 760 mmHg 
  • Flash Point:282.5°C 
  • Density:1.605g/cm3 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:2
  • Exact Mass:333.06372245
  • Heavy Atom Count:25
  • Complexity:615
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=C(C(=N2)C3=C(C4=C(C3=O)C=CC(=C4)C(=O)O)O)O
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