1. Home
  2. PEPPSI(TM)-SIPr catalyst

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)-

PEPPSI(TM)-SIPr catalyst

CC(c1cccc(c1N1C=CN(C1)c1c(cccc1C(C)C)C(C)C)C(C)C)C.Clc1cccnc1.Cl[Pd]Cl Request for Quotation
Chemical Name: PEPPSI(TM)-SIPr catalyst
CAS Number: 927706-57-8
Product Number: AG003BEP(AGN-PC-0WAES1)
Synonyms:
MDL No:
Molecular Formula: C32H42Cl3N3Pd
Molecular Weight: 681.4750

Identification/Properties

Properties
MP:
198-201℃ (分解)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
681.479g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
679.148g/mol
Monoisotopic Mass:
679.148g/mol
Topological Polar Surface Area:
19.4A^2
Heavy Atom Count:
39
Formal Charge:
0
Complexity:
516
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

Request for Quotation

Customer Feedback

Chemical Structure


The compound $name$ is a versatile catalyst commonly utilized in chemical synthesis processes. Specifically, it is employed as a palladium-based catalyst in various organic transformations due to its ability to facilitate coupling reactions efficiently. This catalyst plays a crucial role in promoting C-C and C-N bond formations, enabling the synthesis of complex organic molecules with high selectivity and yields. Its unique structure allows for enhanced reactivity and control in diverse transformations, including cross-coupling reactions, amination reactions, and carbon-carbon bond formations. Overall, $name$ serves as a powerful tool in modern organic synthesis, contributing to the development of new materials and pharmaceuticals through its catalytic properties.