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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)-

Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-9-oxo-, (5Z,8b,13E,15S)-

CCCCC[C@@H](/C=C/[C@H]1C=CC(=O)[C@H]1C/C=CCCCC(=O)O)O Request for Quotation
Chemical Name: Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-9-oxo-, (5Z,8b,13E,15S)-
CAS Number: 474391-66-7
Product Number: AG00DAA7(AGN-PC-0OAL9Z)
Synonyms:
MDL No:
Molecular Formula: C20H30O4
Molecular Weight: 334.4498

Identification/Properties

Computed Properties
Molecular Weight:
334.456g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
12
Exact Mass:
334.214g/mol
Monoisotopic Mass:
334.214g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
476
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
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


Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-9-oxo-, (5Z,8b,13E,15S) is a key intermediate utilized in various chemical synthesis processes. This compound plays a crucial role in the creation of a diverse range of pharmaceuticals, agrochemicals, and advanced materials. Specifically, it serves as a vital building block in the synthesis of bioactive molecules, where its unique structure and functional groups enable the formation of complex chemical structures. By strategically incorporating Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-9-oxo-, (5Z,8b,13E,15S) into synthesis pathways, chemists can access novel compounds with enhanced biological activities and tailored properties, making it an indispensable tool in the realm of chemical synthesis.