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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, 7-amino-3,4-dihydro-

Nc1cc2NC(=O)CCc2cc1 Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 7-amino-3,4-dihydro-
CAS Number: 22246-07-7
Product Number: AG00BDFI(AGN-PC-0LOCF1)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O
Molecular Weight: 162.1885

Identification/Properties

Properties
MP:
213-214℃
BP:
403.1°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
162.192g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
162.079g/mol
Monoisotopic Mass:
162.079g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Used as a versatile building block in chemical synthesis, 7-Amino-3,4-dihydro-2(1H)-quinolinone is a key intermediate that plays a crucial role in the creation of various organic compounds. This compound serves as a valuable starting material in the development of pharmaceuticals, agrochemicals, and materials science. With its unique structural properties, 7-Amino-3,4-dihydro-2(1H)-quinolinone enables chemists to efficiently access a wide range of structurally diverse molecules. Its ability to undergo various functional group transformations makes it an indispensable tool for the synthesis of complex organic compounds with high efficiency and precision.