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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-oxo-1,3-dihydroindole-4-carbonitrile

N#Cc1cccc2c1CC(=O)N2 Request for Quotation
Chemical Name: 2-oxo-1,3-dihydroindole-4-carbonitrile
CAS Number: 214759-51-0
Product Number: AG003HTZ(AGN-PC-03UGDU)
Synonyms:
MDL No: MFCD20480663
Molecular Formula: C9H6N2O
Molecular Weight: 158.1567

Identification/Properties

Properties
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Oxoindoline-4-carbonitrile is a versatile compound widely used in chemical synthesis as a key building block. Its unique structure and reactivity make it an essential component in the development of various organic compounds. One of the main applications of 2-Oxoindoline-4-carbonitrile is its utility as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, this compound serves as a valuable intermediate in the production of dyes, pigments, and complex organic molecules. Its ability to undergo various reactions, such as cyclization, alkylation, and condensation, make it a valuable tool for chemists in creating diverse and complex molecular structures. The versatile nature of 2-Oxoindoline-4-carbonitrile makes it an indispensable component in the modern organic synthesis toolbox.