(15R)-BiMatoprost|1163135-92-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

(15R)-BiMatoprost

CCNC(=O)CCCC=CC[C@H]1[C@@H](O)C[C@H]([C@@H]1/C=C/[C@@H](CCc1ccccc1)O)O

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Chemical Name:	(15R)-BiMatoprost
CAS Number:	1163135-92-9
Product Number:	AG008SQX(AGN-PC-0WA1LW)
Synonyms:
MDL No:
Molecular Formula:	C25H37NO4
Molecular Weight:	415.56558

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Identification/Properties

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Chemical Structure

The application of (15R)-Bimatoprost in chemical synthesis lies predominantly in its role as a key intermediate in the production of prostaglandin analogs, specifically those used in glaucoma treatment. By utilizing (15R)-Bimatoprost as a starting material, chemists can perform various transformations and modifications to ultimately yield compounds with enhanced pharmacological properties and improved therapeutic efficacy. Its unique stereochemistry and functional groups make (15R)-Bimatoprost a versatile building block for the synthesis of novel prostaglandin derivatives, paving the way for the development of next-generation ocular medications and other bioactive molecules.