Home Other Building Blocks 5-Fluoroindoline-2,3-dione

5-Fluoroindoline-2,3-dione

CAS No.:
443-69-6
Catalog Number:
AG00349V
Molecular Formula:
C8H4FNO2
Molecular Weight:
165.1213
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$10
- +
25g
97%
In Stock USA
United States
$44
- +
100g
97%
In Stock USA
United States
$119
- +
250g
98%(GC)
In Stock USA
United States
$258
- +
500g
97%
In Stock USA
United States
$475
- +
Product Description
Catalog Number:
AG00349V
Chemical Name:
5-Fluoroindoline-2,3-dione
CAS Number:
443-69-6
Molecular Formula:
C8H4FNO2
Molecular Weight:
165.1213
MDL Number:
MFCD00022795
IUPAC Name:
5-fluoro-1H-indole-2,3-dione
InChI:
InChI=1S/C8H4FNO2/c9-4-1-2-6-5(3-4)7(11)8(12)10-6/h1-3H,(H,10,11,12)
InChI Key:
GKODDAXOSGGARJ-UHFFFAOYSA-N
SMILES:
Fc1ccc2c(c1)C(=O)C(=O)N2
NSC Number:
39161
Properties
Complexity:
241  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
165.023g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
165.123g/mol
Monoisotopic Mass:
165.023g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
46.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
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(Z)-2-(5-Fluoro-2-oxoindolin-3-yl-idene)-N-phenyl-hydrazinecarbothio-amide. Acta crystallographica. Section E, Structure reports online 20120201
Chemical synthesis, in vitro acetohydroxyacid synthase (AHAS) inhibition, herbicidal activity, and computational studies of isatin derivatives. Journal of agricultural and food chemistry 20110928
5-Fluoro-1-(4-meth-oxy-benz-yl)indoline-2,3-dione. Acta crystallographica. Section E, Structure reports online 20110701
5''-(4-Chloro-benzyl-idene)-4'-(4-chloro-phen-yl)-5-fluoro-1',1''-dimethyl-indoline-3-spiro-2'-pyrrolidine-3'-spiro-3''-piperidine-2,4''-dione. Acta crystallographica. Section E, Structure reports online 20110401
Synthesis of 3,3-diindolyl oxyindoles efficiently catalysed by FeCl3 and their in vitro evaluation for anticancer activity. Bioorganic & medicinal chemistry letters 20100901
QSAR study of isatin analogues as in vitro anti-cancer agents. European journal of medicinal chemistry 20100301
Synthesis and Pharmacological Evaluation of Novel Schiff Base Analogues of 3-(4-amino) Phenylimino) 5-fluoroindolin-2-one. Journal of young pharmacists : JYP 20100101
Investigation of trypanothione reductase as a drug target in Trypanosoma brucei. ChemMedChem 20091207
N'-(5-Fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl-idene)benzene-sulfono-hydrazide. Acta crystallographica. Section E, Structure reports online 20080501
Synthesis and structure-antituberculosis activity relationship of 1H-indole-2,3-dione derivatives. Bioorganic & medicinal chemistry 20070901
Synthesis, antibacterial, antifungal and antiviral activity evaluation of some new bis-Schiff bases of isatin and their derivatives. Molecules (Basel, Switzerland) 20070807
Biological targets for isatin and its analogues: Implications for therapy. Biologics : targets & therapy 20070601
Selective inhibition of carboxylesterases by isatins, indole-2,3-diones. Journal of medicinal chemistry 20070419
In vitro cytotoxicity evaluation of some substituted isatin derivatives. Bioorganic & medicinal chemistry 20070115
Synthesis of some new bis-Schiff bases of isatin and 5-fluoroisatin in a water suspension medium. Molecules (Basel, Switzerland) 20060131
Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain. Bioorganic & medicinal chemistry letters 20031020
Synthesis and antiviral evaluation of isatin ribonucleosides. Nucleosides, nucleotides & nucleic acids 20020101
Properties