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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)-

6-methyl-3,4-dihydro-2H-isoquinolin-1-one

Cc1ccc2c(c1)CCNC2=O Request for Quotation
Chemical Name: 6-methyl-3,4-dihydro-2H-isoquinolin-1-one
CAS Number: 1082041-78-8
Product Number: AG00HB3G(AGN-PC-03WAKB)
Synonyms:
MDL No:
Molecular Formula: C10H11NO
Molecular Weight: 161.2004

Identification/Properties

Computed Properties
Molecular Weight:
161.204g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
161.084g/mol
Monoisotopic Mass:
161.084g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
190
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


6-Methyl-3,4-dihydroisoquinolin-1(2H)-one is a valuable compound used in chemical synthesis for the preparation of various organic molecules. This versatile building block plays a crucial role in the formation of complex structures due to its unique molecular properties. In particular, it serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. By incorporating 6-Methyl-3,4-dihydroisoquinolin-1(2H)-one into chemical reactions, chemists can access a wide range of structurally diverse compounds with potential applications in drug discovery and material science. Its strategic placement within synthetic pathways enables the efficient construction of intricate molecular frameworks, making it a valuable tool for synthetic chemists seeking to develop novel compounds with tailored properties.