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1861-29-6

1861-29-6 | 2H-Indol-2-one,1,3-dihydro-3-methylene-

CAS No: 1861-29-6 Catalog No: AG0076AX MDL No:

Product Description

Catalog Number:
AG0076AX
Chemical Name:
2H-Indol-2-one,1,3-dihydro-3-methylene-
CAS Number:
1861-29-6
Molecular Formula:
C9H7NO
Molecular Weight:
145.1580
IUPAC Name:
3-methylidene-1H-indol-2-one
InChI:
InChI=1S/C9H7NO/c1-6-7-4-2-3-5-8(7)10-9(6)11/h2-5H,1H2,(H,10,11)
InChI Key:
IGXUUWYVUGBMFT-UHFFFAOYSA-N
SMILES:
C=C1C(=O)Nc2c1cccc2

Properties

Complexity:
210  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
145.053g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
145.161g/mol
Monoisotopic Mass:
145.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
29.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  

Literature

Title Journal
Seven 3-methylidene-1H-indol-2(3H)-ones related to the multiple-receptor tyrosine kinase inhibitor sunitinib. Acta crystallographica. Section C, Crystal structure communications 20100201
Palladium-catalyzed intramolecular 5-exo-dig hydroarylations of N-arylpropiolamides: thermodynamics-controlled stereoselective synthesis of 3-methyleneoxindoles. The Journal of organic chemistry 20091120
Organocatalytic synthesis of spiro[pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity. Journal of the American Chemical Society 20090930
Synthesis of (2-oxoindolin-3-ylidene)methyl acetates involving a C-H functionalization process. Organic letters 20080501
Total synthesis of (+/-)-alantrypinone by hetero Diels-Alder reaction. The Journal of organic chemistry 20040109
3-Methyleneoxindole: an affinity label of glutathione S-transferase pi which targets tryptophan 38. Biochemistry 20010626

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