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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)-

AHU-377 (Sacubitril) - 149709-62-6 or AHU-377 (Sacubitril) calcium

CCOC(=O)[C@@H](C[C@@H](Cc1ccc(cc1)c1ccccc1)NC(=O)CCC(=O)[O-])C.CCOC(=O)[C@@H](C[C@@H](Cc1ccc(cc1)c1ccccc1)NC(=O)CCC(=O)[O-])C.[Ca+2] Request for Quotation
Chemical Name: AHU-377 (Sacubitril) - 149709-62-6 or AHU-377 (Sacubitril) calcium
CAS Number: 1369773-39-6
Product Number: AG0012M5(AGN-PC-0WAJXE)
Synonyms:
MDL No:
Molecular Formula: C48H56CaN2O10
Molecular Weight: 861.0436

Identification/Properties

Computed Properties
Molecular Weight:
861.058g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
22
Exact Mass:
860.356g/mol
Monoisotopic Mass:
860.356g/mol
Topological Polar Surface Area:
191A^2
Heavy Atom Count:
61
Formal Charge:
0
Complexity:
544
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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

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Chemical Structure


The application of Calcium 4-(((2S,4R)-1-([1,1'-biphenyl]-4-yl)-5-ethoxy-4-methyl-5-oxopentan-2-yl)amino)-4-oxobutanoate in chemical synthesis involves its utilization as a versatile reagent for the formation of complex organic compounds. This compound serves as a key building block in the assembly of various pharmaceuticals, agrochemicals, and natural products. By incorporating Calcium 4-(((2S,4R)-1-([1,1'-biphenyl]-4-yl)-5-ethoxy-4-methyl-5-oxopentan-2-yl)amino)-4-oxobutanoate into chemical reactions, chemists can access structurally diverse molecules with enhanced biological activities and tailored properties. Its strategic placement within a synthetic pathway enables selective functional group transformations, stereoselective reactions, and efficient bond formations, thereby facilitating the synthesis of intricate molecular structures for advanced applications in drug discovery, materials science, and chemical biology.