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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)-

R788 disodium hexahydrate

COc1cc(Nc2ncc(c(n2)Nc2ccc3c(n2)N(COP(=O)([O-])[O-])C(=O)C(O3)(C)C)F)cc(c1OC)OC.[Na+].[Na+].O.O.O.O.O.O Request for Quotation
Chemical Name: R788 disodium hexahydrate
CAS Number: 914295-16-2
Product Number: AG00GU60(AGN-PC-0WAMDU)
Synonyms:
MDL No:
Molecular Formula: C23H36FN6Na2O15P
Molecular Weight: 732.5148

Identification/Properties

Computed Properties
Molecular Weight:
732.52g/mol
Hydrogen Bond Donor Count:
8
Hydrogen Bond Acceptor Count:
21
Rotatable Bond Count:
9
Exact Mass:
732.176g/mol
Monoisotopic Mass:
732.176g/mol
Topological Polar Surface Area:
198A^2
Heavy Atom Count:
48
Formal Charge:
0
Complexity:
893
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:
9
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


R788 disodium hexahydrate is a versatile compound commonly used in chemical synthesis due to its unique properties and role as a key reactant. In the realm of organic chemistry, specifically for the synthesis of pharmaceutical intermediates and fine chemicals, R788 disodium hexahydrate serves as a crucial reagent for various transformations and reactions.Its ability to serve as an efficient catalyst in a range of organic transformations, such as oxidation and reduction reactions, makes it an indispensable tool in the hands of synthetic chemists. The compound's solubility in both organic solvents and water further enhances its utility in diverse reaction conditions, allowing for flexibility and compatibility in different experimental setups.Additionally, R788 disodium hexahydrate's stability and controlled reactivity make it an ideal choice for promoting selective bond formation and functional group manipulations in complex chemical reactions. Its involvement in key synthetic steps contributes to the synthesis of intricate molecular structures with high yields and purity, making it a valuable component in the toolkit of synthetic chemists worldwide.Overall, the application of R788 disodium hexahydrate in chemical synthesis extends beyond its role as a mere reagent, showcasing its significance in facilitating the efficient and precise construction of important organic molecules for various industrial and academic purposes.