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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)-

Prostaglandin E<sub>2</sub> methyl ester

CCCCCC(/C=C/[C@H]1C(O)CC(=O)C1CC=CCCCC(=O)OC)O Request for Quotation
Chemical Name: Prostaglandin E<sub>2</sub> methyl ester
CAS Number: 31753-17-0
Product Number: AG007IO5(AGN-PC-0WAIR5)
Synonyms:
MDL No:
Molecular Formula: C21H34O5
Molecular Weight: 366.4917

Identification/Properties

Computed Properties
Molecular Weight:
366.498g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
13
Exact Mass:
366.241g/mol
Monoisotopic Mass:
366.241g/mol
Topological Polar Surface Area:
83.8A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
483
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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


PGE2 methyl ester, also known as Prostaglandin E2 methyl ester, is a key compound used in chemical synthesis for various applications. This compound serves as a versatile building block in organic synthesis, particularly in the pharmaceutical industry. Its unique structural properties make it a valuable component in the creation of novel drug compounds and pharmaceutical intermediates. In addition, PGE2 methyl ester can be utilized in the development of advanced materials and agrochemicals, showcasing its wide-ranging utility in the field of chemistry. Its compatibility with diverse reaction conditions and its ability to undergo various chemical transformations make it a valuable tool for synthetic chemists looking to design and produce complex molecules with specific biological activities.