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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)-Quinoxalinone, 3,4-dihydro-3-methyl-

CC1Nc2ccccc2NC1=O Request for Quotation
Chemical Name: 2(1H)-Quinoxalinone, 3,4-dihydro-3-methyl-
CAS Number: 34070-68-3
Product Number: AG00C8W8(AGN-PC-0KKPOE)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O
Molecular Weight: 162.1885

Identification/Properties

Computed Properties
Molecular Weight:
162.192g/mol
XLogP3:
1.3
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:
41.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H319-H413
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methyl-3,4-dihydro-2(1H)-quinoxalinone, also known as $name$, is a versatile compound widely used in chemical synthesis. One of its key applications is as a building block in the synthesis of biologically active molecules such as pharmaceuticals and agrochemicals. Due to its unique structural features, $name$ serves as an important intermediate in the preparation of various heterocyclic compounds. Its presence in the chemical synthesis process allows for the modification of molecular structures to enhance desired properties or activities. Additionally, $name$ can be utilized in the creation of novel materials with specific functionalities, making it an essential component in the toolkit of synthetic chemists.