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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)-

NVP-BHG712

Cc1ccc(cc1Nc1nc(nc2c1cnn2C)c1cccnc1)C(=O)Nc1cccc(c1)C(F)(F)F Request for Quotation
Chemical Name: NVP-BHG712
CAS Number: 940310-85-0
Product Number: AG00GU50(AGN-PC-0W3NSH)
Synonyms:
MDL No:
Molecular Formula: C26H20F3N7O
Molecular Weight: 503.4785

Identification/Properties

Computed Properties
Molecular Weight:
503.489g/mol
XLogP3:
4.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
5
Exact Mass:
503.168g/mol
Monoisotopic Mass:
503.168g/mol
Topological Polar Surface Area:
97.6A^2
Heavy Atom Count:
37
Formal Charge:
0
Complexity:
786
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 4-Methyl-3-((1-methyl-6-(pyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino)-N-(3-(trifluoromethyl)phenyl)benzamide, also known as $name$, finds application in chemical synthesis as a potent building block. It serves as a versatile intermediate in organic synthesis, allowing for the generation of complex molecular structures with specific functionalities. This compound is particularly valuable in the creation of novel pharmaceuticals, agrochemicals, and materials due to its unique chemical properties and reactivity. Its strategic placement of functional groups enables the formation of key bonds and scaffolds essential for the development of advanced molecular frameworks. By incorporating $name$ into synthetic pathways, chemists can efficiently access a diverse array of compounds with tailored properties and applications.