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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)-

TM5441

O=C(Nc1cccc(c1)c1ccco1)COCC(=O)Nc1ccc(cc1C(=O)O)Cl Request for Quotation
Chemical Name: TM5441
CAS Number: 1190221-43-2
Product Number: AG01EOE2(AGN-PC-3H46C5)
Synonyms:
MDL No:
Molecular Formula: C21H17ClN2O6
Molecular Weight: 428.8225

Identification/Properties

Computed Properties
Molecular Weight:
428.825g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
428.078g/mol
Monoisotopic Mass:
428.078g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
618
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


TM-5441 is a versatile compound commonly used in chemical synthesis for its ability to act as a potent catalyst in a wide range of organic transformations. This innovative catalyst has demonstrated remarkable efficacy in promoting various chemical reactions, including cross-coupling reactions, asymmetric transformations, and tandem reactions.Its unique structure and composition enable TM-5441 to drive reactions with high efficiency and selectivity, making it an indispensable tool for synthetic chemists seeking to access complex molecular structures. Whether it's facilitating the formation of C-C, C-N, or C-O bonds, TM-5441 consistently delivers exceptional performance, even in challenging reaction conditions.Moreover, the versatility of TM-5441 extends to its compatibility with a diverse array of substrates, allowing chemists to explore diverse synthetic pathways with confidence. From drug discovery to material science, the applications of TM-5441 in chemical synthesis are vast and continuously expanding, positioning it as a valuable asset in the toolbox of modern organic chemistry.