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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)-

3H-Indol-3-one, 1-acetyl-1,2-dihydro-

CC(=O)N1CC(=O)c2c1cccc2 Request for Quotation
Chemical Name: 3H-Indol-3-one, 1-acetyl-1,2-dihydro-
CAS Number: 16800-68-3
Product Number: AG0037ZH(AGN-PC-0JSK4N)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

Identification/Properties

Computed Properties
Molecular Weight:
175.187g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
175.063g/mol
Monoisotopic Mass:
175.063g/mol
Topological Polar Surface Area:
37.4A^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


1-Acetylindolin-3-one, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound serves as a valuable building block in the development of various organic molecules with important applications in pharmaceuticals, materials science, and agrochemicals.As a key intermediate in the synthesis of indole-based compounds, 1-Acetylindolin-3-one plays a crucial role in the preparation of biologically active molecules such as pharmaceutical drugs and natural products. Its ability to undergo diverse chemical transformations, including functional group modifications and heterocyclic ring formations, makes it an essential component in the creation of complex molecular structures.In the field of medicinal chemistry, 1-Acetylindolin-3-one is utilized for the synthesis of novel drug candidates with potential therapeutic properties. By incorporating this compound into drug design strategies, chemists can explore new chemical space and develop innovative pharmaceutical agents targeting various diseases and disorders.Furthermore, in materials science, 1-Acetylindolin-3-one is employed in the design and fabrication of advanced materials with tailored properties. Its structural features enable the construction of functionalized materials for electronic applications, organic semiconductors, and nanotechnology-based devices, offering a platform for cutting-edge research and technological advancements.Moreover, in agrochemical research, 1-Acetylindolin-3-one serves as a precursor for the synthesis of bioactive molecules used in the development of crop protection agents and pesticides. Its structural versatility allows for the design of environmentally friendly and potent agrochemicals that contribute to sustainable agricultural practices and pest management strategies.Overall, the application of 1-Acetylindolin-3-one in chemical synthesis encompasses a wide range of disciplines, highlighting its significance in shaping the field of organic chemistry and enabling the creation of diverse molecules with important functions and applications.