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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)-

6,7-dimethoxy-2-methyl-4-phenyl-3,4-dihydro-1H-isoquinoline

COc1cc2c(cc1OC)CN(CC2c1ccccc1)C Request for Quotation
Chemical Name: 6,7-dimethoxy-2-methyl-4-phenyl-3,4-dihydro-1H-isoquinoline
CAS Number: 128942-65-4
Product Number: AG000YOW(AGN-PC-003SS1)
Synonyms:
MDL No:
Molecular Formula: C18H21NO2
Molecular Weight: 283.3648

Identification/Properties

Computed Properties
Molecular Weight:
283.371g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
283.157g/mol
Monoisotopic Mass:
283.157g/mol
Topological Polar Surface Area:
21.7A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
329
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dimethoxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline is a versatile organic compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in the creation of various complex organic molecules due to its unique structure and reactivity. In chemical synthesis, 6,7-Dimethoxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline can be used as a key intermediate in the production of pharmaceuticals, agrochemicals, and functional materials. Its functional groups allow for further manipulation through various chemical reactions, enabling the formation of more intricate and advanced compounds. The compound's structural properties make it a valuable tool for organic chemists seeking to design and construct novel organic molecules with specific desired traits and applications.