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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)-

ML345

Fc1ccc2c(c1)c(=O)n(s2)c1cc(ccc1N1CCOCC1)S(=O)(=O)N1CCOCC1 Request for Quotation
Chemical Name: ML345
CAS Number: 1632125-79-1
Product Number: AG01E0MM(AGN-PC-0WP0OK)
Synonyms:
MDL No:
Molecular Formula: C21H22FN3O5S2
Molecular Weight: 479.5449

Identification/Properties

Computed Properties
Molecular Weight:
479.541g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
4
Exact Mass:
479.098g/mol
Monoisotopic Mass:
479.098g/mol
Topological Polar Surface Area:
113A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
785
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


ML 345 is a versatile organic compound widely used in modern chemical synthesis, particularly in the field of medicinal chemistry and drug discovery. With its unique structural properties and reactivity, ML 345 serves as a valuable building block for the efficient synthesis of various biologically active molecules.One of the key applications of ML 345 in chemical synthesis is its role as a versatile precursor for the functionalization of complex organic molecules. Its ability to undergo diverse chemical reactions, such as cross-coupling reactions, oxidation, and reduction, enables chemists to efficiently modify the structure of target compounds and create novel analogs with improved biological activities.Furthermore, ML 345 plays a crucial role in the construction of intricate molecular frameworks through its use in multi-step synthesis strategies. By incorporating ML 345 at strategic points in a synthetic route, chemists can streamline the synthesis of complex natural products and pharmaceutical compounds, saving time and resources in the process.Overall, the application of ML 345 in chemical synthesis offers chemists a powerful tool to access a wide range of structurally diverse and biologically relevant compounds, making it an indispensable component of modern drug discovery and development efforts.