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Home > Indoles and Oxindole > 45738-06-5
45738-06-5 | 1H-Isoindol-1-one
CAS No: 45738-06-5 Catalog No: AG006YSZ MDL No:
Product Description
Catalog Number:
AG006YSZ
Chemical Name:
1H-Isoindol-1-one
CAS Number:
45738-06-5
Molecular Formula:
C8H5NO
Molecular Weight:
131.1314
IUPAC Name:
isoindol-1-one
InChI:
InChI=1S/C8H5NO/c10-8-7-4-2-1-3-6(7)5-9-8/h1-5H
InChI Key:
XTBAPWCYTNCZTO-UHFFFAOYSA-N
SMILES:
O=C1N=Cc2c1cccc2
Properties
Complexity:
186
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
131.037g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
131.134g/mol
Monoisotopic Mass:
131.037g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
29.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1
Literature
| Title | Journal |
|---|---|
| Rh(I)-catalyzed asymmetric synthesis of 3-substituted isoindolinones through CO gas-free aminocarbonylation. | The Journal of organic chemistry 20120316 |
| Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum. | Phytochemistry 20110801 |
| Antiproliferative lactams and spiroenone from adlay bran in human breast cancer cell lines. | Journal of agricultural and food chemistry 20110223 |
| Progress in the developement of positive allosteric modulators of the metabotropic glutamate receptor 2. | Current medicinal chemistry 20110101 |
| Synthesis and nootropic activity of some 2,3-dihydro-1H-isoindol-1-one derivatives structurally related with piracetam. | Chemistry & biodiversity 20101101 |
| 6-Alkoxyisoindolin-1-one based dopamine D2 partial agonists as potential antipsychotics. | Bioorganic & medicinal chemistry letters 20101001 |
| 3-Eth-oxy-2-(1,3-thia-zol-2-yl)isoindolin-1-one. | Acta crystallographica. Section E, Structure reports online 20091001 |
| Diketoacid-genre HIV-1 integrase inhibitors containing enantiomeric arylamide functionality. | Bioorganic & medicinal chemistry 20090715 |
| A tetrachloro polyketide hexahydro-1H-isoindolone, muironolide A, from the marine sponge Phorbas sp. natural products at the nanomole scale. | Journal of the American Chemical Society 20090610 |
| Regioselective synthesis of N-aminoisoindolones and mono-N- and di-N,N'-substituted phthalazones utilizing hydrazine nucleophiles in a palladium-catalyzed three-component cascade process. | The Journal of organic chemistry 20081107 |
| [(18)F]-labeled isoindol-1-one and isoindol-1,3-dione derivatives as potential PET imaging agents for detection of beta-amyloid fibrils. | Bioorganic & medicinal chemistry letters 20081015 |
| Isoindol-1,3-dione and isoindol-1-one derivatives with high binding affinity to beta-amyloid fibrils. | Bioorganic & medicinal chemistry letters 20080301 |
| Solution-phase parallel synthesis of hexahydro-1H-isoindolone libraries via tactical combination of Cu-catalyzed three-component coupling and Diels-Alder reactions. | Journal of combinatorial chemistry 20080101 |
| Copper-catalyzed multicomponent cascade process for the synthesis of hexahydro-1H-isoindolones. | The Journal of organic chemistry 20070216 |
| Synthesis and mixed lineage kinase activity of pyrrolocarbazole and isoindolone analogs of (+)K-252a. | Journal of medicinal chemistry 20070208 |
| Isoindolone derivatives, a new class of 5-HT2C antagonists: synthesis and biological evaluation. | Bioorganic & medicinal chemistry letters 20070115 |
| Synthesis, proton and 13C NMR and reaction mechanism studies of novel isoindolones derivatives, obtained through TAWERS procedure. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20050901 |
| The discovery and synthesis of novel adenosine substituted 2,3-dihydro-1H-isoindol-1-ones: potent inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1). | Bioorganic & medicinal chemistry letters 20040105 |
| Synthesis and investigation of conformationally restricted analogues of lavendustin A as cytotoxic inhibitors of tubulin polymerization. | Journal of medicinal chemistry 20021010 |
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