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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)-

4(1H)-Quinolinone, 7-chloro-2,3-dihydro-

Clc1ccc2c(c1)NCCC2=O Request for Quotation
Chemical Name: 4(1H)-Quinolinone, 7-chloro-2,3-dihydro-
CAS Number: 21617-15-2
Product Number: AG0037KD(AGN-PC-0JLXS2)
Synonyms:
MDL No:
Molecular Formula: C9H8ClNO
Molecular Weight: 181.6189

Identification/Properties

Properties
MP:
130-132°C
BP:
340.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
181.619g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
181.029g/mol
Monoisotopic Mass:
181.029g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
195
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-Chloro-2,3-dihydroquinolin-4(1H)-one, also known by its chemical formula C9H8ClNO, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it an essential building block for the creation of various organic compounds.In chemical synthesis, this compound serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its chlorinated quinoline ring system provides a platform for further derivatization, allowing for the introduction of different functional groups to tailor the final compound's properties.One common application of 7-Chloro-2,3-dihydroquinolin-4(1H)-one is in the synthesis of biologically active molecules, such as antimalarials, antibacterials, and anticancer agents. By incorporating this compound into the molecular structure, chemists can access a wide range of potential pharmacological activities.Additionally, 7-Chloro-2,3-dihydroquinolin-4(1H)-one can be used in the preparation of high-performance materials, such as polymers, dyes, and organic light-emitting diodes (OLEDs). Its versatile reactivity and compatibility with various reaction conditions make it a valuable tool in the development of advanced materials with tailored properties.Overall, the strategic placement of the chloro substituent on the quinoline scaffold of 7-Chloro-2,3-dihydroquinolin-4(1H)-one makes it a key player in the realm of chemical synthesis, offering endless possibilities for creating new and innovative compounds with diverse applications.