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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(1H)-Quinolinone, 8-chloro-3,4-dihydro-4,4-dimethyl-

O=C1Nc2c(Cl)cccc2C(C1)(C)C Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 8-chloro-3,4-dihydro-4,4-dimethyl-
CAS Number: 676116-21-5
Product Number: AG00FGYX(AGN-PC-09RRVO)
Synonyms:
MDL No:
Molecular Formula: C11H12ClNO
Molecular Weight: 209.6721

Identification/Properties

Computed Properties
Molecular Weight:
209.673g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
209.061g/mol
Monoisotopic Mass:
209.061g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
252
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


8-Chloro-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one, also known as $name$, serves as a versatile chemical building block in organic synthesis. This compound is widely used in the development of pharmaceuticals, agrochemicals, and materials due to its unique structural characteristics.In chemical synthesis, $name$ acts as a key intermediate in the preparation of various biologically active molecules. Its chlorinated quinoline framework provides a valuable scaffold for the introduction of different functional groups through synthetic transformations. This allows for the fine-tuning of properties such as solubility, reactivity, and bioavailability in target molecules.Moreover, the presence of the 8-chloro substituent in $name$ enables selective functionalization reactions, leading to the formation of diverse chemical entities with specific activities. By strategically incorporating this moiety into molecular structures, chemists can modulate the biological interactions and pharmacological profiles of the final compounds.Overall, the application of 8-Chloro-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one in chemical synthesis showcases its significance as a valuable tool for designing novel compounds with potential applications in drug discovery, crop protection, and materials science.