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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)-

1H-Indole-2,3-dione, 7-ethyl-

CCc1cccc2c1NC(=O)C2=O Request for Quotation
Chemical Name: 1H-Indole-2,3-dione, 7-ethyl-
CAS Number: 79183-65-6
Product Number: AG005A0M(AGN-PC-0JOJWB)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
175.187g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
175.063g/mol
Monoisotopic Mass:
175.063g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
249
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Ethylindoline-2,3-dione is a versatile compound that finds significant application in chemical synthesis, particularly in organic chemistry. This compound serves as a valuable building block for the synthesis of various organic molecules due to its unique structure and reactivity.One key application of 7-Ethylindoline-2,3-dione is its use as a precursor in the synthesis of heterocyclic compounds. By undergoing various chemical transformations, this compound can be employed to create complex heterocycles with diverse functionalities. These heterocyclic compounds have widespread applications in pharmaceuticals, agrochemicals, and materials science.Additionally, 7-Ethylindoline-2,3-dione can participate in various multicomponent reactions to generate structurally diverse compounds. Its reactivity allows for the introduction of different functional groups, enabling the synthesis of novel molecules with tailored properties.Furthermore, this compound can be utilized in the development of new synthetic methodologies and the construction of bioactive molecules. Its involvement in cascade reactions and asymmetric synthesis further highlights its importance in modern organic chemistry research.Overall, the versatility and reactivity of 7-Ethylindoline-2,3-dione make it a valuable tool for chemical synthesis, offering opportunities for the creation of intricate organic molecules with potential applications across various disciplines.