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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)-

5-Heptenoic acid,7-[3,5-dihydroxy-2-(3-hydroxy-5-phenyl-1-pentenyl)cyclopentyl]-,1-methylethyl ester, [1R-[1a(Z),2b(1E,3R*),3a,5a]]-

CC(OC(=O)CCC/C=CC[C@H]1[C@@H](O)C[C@H]([C@@H]1/C=C/[C@@H](CCc1ccccc1)O)O)C Request for Quotation
Chemical Name: 5-Heptenoic acid,7-[3,5-dihydroxy-2-(3-hydroxy-5-phenyl-1-pentenyl)cyclopentyl]-,1-methylethyl ester, [1R-[1a(Z),2b(1E,3R*),3a,5a]]-
CAS Number: 130273-87-9
Product Number: AG000U77(AGN-PC-0PJ78H)
Synonyms:
MDL No:
Molecular Formula: C26H38O5
Molecular Weight: 430.5769

Identification/Properties

Computed Properties
Molecular Weight:
430.585g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
13
Exact Mass:
430.272g/mol
Monoisotopic Mass:
430.272g/mol
Topological Polar Surface Area:
87A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
564
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
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


15(R)-Bimatoprost isopropyl ester, a derivative of the prostaglandin F2α analog bimatoprost, is a valuable compound in chemical synthesis. Its primary application lies in its role as a key intermediate in the manufacturing of pharmaceutical compounds, particularly in the synthesis of drugs used for the treatment of glaucoma and other ophthalmic conditions. In organic chemistry, 15(R)-Bimatoprost isopropyl ester serves as a crucial building block for the creation of novel prostaglandin derivatives and related bioactive molecules. Its structural features make it a versatile starting material for the development of analogs with improved pharmacological properties or altered biological activities. Furthermore, the unique stereochemistry of the 15(R) configuration in this compound plays a significant role in determining its reactivity and interactions with other molecules during synthetic processes. Overall, the strategic incorporation of 15(R)-Bimatoprost isopropyl ester in chemical synthesis allows for the efficient production of advanced pharmaceuticals with enhanced therapeutic potential.