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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)-

Pilaralisib (XL-147)

COc1ccc(c(c1)Nc1nc2ccccc2nc1NS(=O)(=O)c1cccc(c1)NC(=O)C(N)(C)C)Cl Request for Quotation
Chemical Name: Pilaralisib (XL-147)
CAS Number: 934526-89-3
Product Number: AG00GU7F(AGN-PC-0WAJVS)
Synonyms:
MDL No:
Molecular Formula: C25H25ClN6O4S
Molecular Weight: 541.0218

Identification/Properties

Computed Properties
Molecular Weight:
541.023g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
8
Exact Mass:
540.135g/mol
Monoisotopic Mass:
540.135g/mol
Topological Polar Surface Area:
157A^2
Heavy Atom Count:
37
Formal Charge:
0
Complexity:
887
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 2-Amino-N-[3-[N-[3-[(2-chloro-5-methoxyphenyl)amino]quinoxalin-2-yl]sulfamoyl]phenyl]-2-methylpropanamide finds significant utility in chemical synthesis processes as a versatile building block. This compound can serve as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural features and functional groups. Its carefully designed molecular structure allows for selective manipulation of its chemical properties, enabling the creation of novel compounds with diverse applications. In synthesis, this compound can participate in a range of reactions such as amide bond formation, halogenation, and sulfonation, facilitating the production of more complex molecules with specific desired characteristics. Its presence in the synthesis pathway can impart crucial functionalities and structural motifs that are vital for the biological activity or physical properties of the final products.