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  2. 7-[(1R,2R,3R)-3-hydroxy-2-[(E)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid

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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)-

7-[(1R,2R,3R)-3-hydroxy-2-[(E)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid

CCCCC[C@@H](/C=C/[C@H]1[C@H](O)CC(=O)[C@H]1CCCCCCC(=O)O)O Request for Quotation
Chemical Name: 7-[(1R,2R,3R)-3-hydroxy-2-[(E)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid
CAS Number: 21003-46-3
Product Number: AG002KJ3(AGN-PC-00AZHB)
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


The (8β,11α,13E,15S)-11,15-Dihydroxy-9-oxoprost-13-en-1-oic acid plays a crucial role in chemical synthesis as a versatile building block due to its unique structure and functional groups. This compound is widely used in the synthesis of various prostaglandin derivatives and analogs, which are important bioactive molecules involved in various physiological processes.Its strategic placement of hydroxyl, ketone, and carboxylic acid functional groups allows for selective chemical modifications to be carried out, enabling the formation of complex molecules with specific pharmacological properties. Furthermore, the presence of a double bond in the carbon chain offers opportunities for stereochemical control during synthesis, leading to compounds with enhanced biological activities.Overall, the (8β,11α,13E,15S)-11,15-Dihydroxy-9-oxoprost-13-en-1-oic acid serves as a valuable intermediate in the preparation of bioactive compounds through controlled chemical transformations, making it an essential component in the field of organic synthesis.