1. Home
  2. Pyrido[2,3-d]pyrimidin-7(8H)-one,6-(2,6-dichlorophenyl)-8-methyl-2-[[3-(methylthio)phenyl]amino]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Pyrido[2,3-d]pyrimidin-7(8H)-one,6-(2,6-dichlorophenyl)-8-methyl-2-[[3-(methylthio)phenyl]amino]-

CSc1cccc(c1)Nc1ncc2c(n1)n(C)c(=O)c(c2)c1c(Cl)cccc1Cl Request for Quotation
Chemical Name: Pyrido[2,3-d]pyrimidin-7(8H)-one,6-(2,6-dichlorophenyl)-8-methyl-2-[[3-(methylthio)phenyl]amino]-
CAS Number: 260415-63-2
Product Number: AG002RGX(AGN-PC-0R1Y1I)
Synonyms:
MDL No:
Molecular Formula: C21H16Cl2N4OS
Molecular Weight: 443.3489

Identification/Properties

Computed Properties
Molecular Weight:
443.346g/mol
XLogP3:
5.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
442.042g/mol
Monoisotopic Mass:
442.042g/mol
Topological Polar Surface Area:
83.4A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
626
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


$Name$ is a potent and selective inhibitor of the atypical protein kinase C (aPKC) isoforms ζ and ι/λ. It has been widely utilized in chemical synthesis as a key catalyst for various transformations, particularly in the context of asymmetric catalysis and cross-coupling reactions. With its unique mode of action, Pd173955 offers significant advantages in the efficient and stereoselective formation of complex molecular structures. In the realm of chemical synthesis, this versatile compound has proven instrumental in enabling the rapid and controlled assembly of diverse organic molecules with high precision and efficacy. Additionally, its compatibility with a broad range of substrates makes Pd173955 a valuable tool for advancing synthetic methodologies and exploring new avenues in modern organic chemistry.