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  2. 1H-Pyrrole-1-heptanoic acid,5-(4-fluorophenyl)-2,3-dihydro-b,d-dihydroxy-3-(1-methylethyl)-2-oxo-4-phenyl-3-[(phenylamino)carbonyl]-, monosodium salt,[3R-[1(bR*,dR*),3R*]]-

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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)-

1H-Pyrrole-1-heptanoic acid,5-(4-fluorophenyl)-2,3-dihydro-b,d-dihydroxy-3-(1-methylethyl)-2-oxo-4-phenyl-3-[(phenylamino)carbonyl]-, monosodium salt,[3R-[1(bR*,dR*),3R*]]-

O[C@@H](C[C@H](CC(=O)[O-])O)CCN1C(=C(C(C1=O)(C(C)C)C(=O)Nc1ccccc1)c1ccccc1)c1ccc(cc1)F.[Na+] Request for Quotation
Chemical Name: 1H-Pyrrole-1-heptanoic acid,5-(4-fluorophenyl)-2,3-dihydro-b,d-dihydroxy-3-(1-methylethyl)-2-oxo-4-phenyl-3-[(phenylamino)carbonyl]-, monosodium salt,[3R-[1(bR*,dR*),3R*]]-
CAS Number: 148217-40-7
Product Number: AG00ADHJ(AGN-PC-0Q1I3S)
Synonyms:
MDL No:
Molecular Formula: C33H34FN2NaO6
Molecular Weight: 596.6210332

Identification/Properties

Computed Properties
Molecular Weight:
596.631g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
12
Exact Mass:
596.23g/mol
Monoisotopic Mass:
596.23g/mol
Topological Polar Surface Area:
130A^2
Heavy Atom Count:
43
Formal Charge:
0
Complexity:
988
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Atorvastatin Lactam Sodium Salt Impurity is a crucial component in chemical synthesis processes, particularly in the pharmaceutical industry. This impurity plays a significant role in the production of Atorvastatin, a widely used medication for managing high cholesterol levels. Through careful manipulation and control of the synthesis pathway, Atorvastatin Lactam Sodium Salt Impurity serves as a key intermediate that facilitates the creation of pure and high-quality Atorvastatin. Its presence enables efficient and reliable manufacturing processes, ensuring the final product meets the required standards for safety and efficacy in treating cardiovascular conditions.