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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)-

Prost-13-en-1-oic acid, 11,15-dihydroxy-9-oxo-, (11a,13E,15R)-

CCCCC[C@H](/C=C/[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(=O)O)O Request for Quotation
Chemical Name: Prost-13-en-1-oic acid, 11,15-dihydroxy-9-oxo-, (11a,13E,15R)-
CAS Number: 20897-91-0
Product Number: AG002JZE(AGN-PC-0O7OKF)
Synonyms:
MDL No:
Molecular Formula: C20H34O5
Molecular Weight: 354.4810

Identification/Properties

Computed Properties
Molecular Weight:
354.487g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
13
Exact Mass:
354.241g/mol
Monoisotopic Mass:
354.241g/mol
Topological Polar Surface Area:
94.8A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
432
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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)-Prostaglandin E1, also known as Alprostadil, plays a crucial role in chemical synthesis due to its ability to act as a versatile building block in the creation of complex organic molecules. This compound is widely utilized in organic chemistry as a chiral starting material for the synthesis of various pharmaceuticals, bioactive compounds, and specialized materials. By serving as a key intermediate in the production of prostaglandin derivatives, 15(R)-Prostaglandin E1 enables chemists to access structurally diverse molecules with tailored biological activities. Moreover, its unique stereochemistry and functional groups make it an ideal candidate for constructing intricate molecular frameworks through strategic synthetic transformations. In the realm of chemical synthesis, 15(R)-Prostaglandin E1 stands as a valuable tool that empowers researchers to design and fabricate novel compounds with enhanced properties and applications.