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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)-

1-phenyl-3,3-bis(pyridin-4-ylmethyl)indol-2-one;dihydrochloride

O=C1N(c2ccccc2)c2c(C1(Cc1ccncc1)Cc1ccncc1)cccc2.Cl.Cl Request for Quotation
Chemical Name: 1-phenyl-3,3-bis(pyridin-4-ylmethyl)indol-2-one;dihydrochloride
CAS Number: 113168-57-3
Product Number: AG01DPWQ(AGN-PC-000PYQ)
Synonyms:
MDL No: MFCD06245587
Molecular Formula: C26H23Cl2N3O
Molecular Weight: 464.3863

Identification/Properties

Computed Properties
Molecular Weight:
464.39g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
463.122g/mol
Monoisotopic Mass:
463.122g/mol
Topological Polar Surface Area:
46.1A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
555
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Linopirdine dihydrochloride, also known as DuP 996, is a pharmaceutical compound frequently utilized as a potassium-channel blocker in various chemical synthesis applications. This compound is valued for its ability to modulate the activity of ion channels, making it a versatile tool in the study of cellular processes and drug development. Linopirdine dihydrochloride has been widely employed in the synthesis of pharmaceutical agents and has shown promising results in improving the efficacy of certain drug formulations. Its precise mechanism of action and favorable pharmacological properties make it a valuable asset in the field of chemical synthesis and medicinal chemistry.