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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)-

5-Heptenoicacid,7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-,1-methylethyl ester, (5E)-

O[C@H](CCc1ccccc1)CC[C@H]1[C@H](O)C[C@@H]([C@@H]1C/C=C/CCCC(=O)OC(C)C)O Request for Quotation
Chemical Name: 5-Heptenoicacid,7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]-,1-methylethyl ester, (5E)-
CAS Number: 913258-34-1
Product Number: AG006OTG(AGN-PC-0VS2WU)
Synonyms:
MDL No:
Molecular Formula: C26H40O5
Molecular Weight: 432.5928

Identification/Properties

Computed Properties
Molecular Weight:
432.601g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
14
Exact Mass:
432.288g/mol
Monoisotopic Mass:
432.288g/mol
Topological Polar Surface Area:
87A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
526
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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


Trans Latanoprost is a valuable compound in chemical synthesis due to its versatile applications. This organic molecule is commonly utilized as a key building block in the synthesis of prostaglandin analogs, which are crucial in the development of pharmaceuticals aimed at treating glaucoma and other ocular diseases.In chemical synthesis, trans Latanoprost serves as a precursor in the construction of these prostaglandin analogs through various reaction pathways. Its functional groups and structural properties make it an ideal starting material for introducing specific modifications and generating structurally diverse analogs with potentially enhanced pharmacological properties.Moreover, the synthetic versatility of trans Latanoprost allows for the exploration of different synthetic strategies and optimization of reaction conditions to access a wide range of analogs with varying biological activities. Its role in chemical synthesis not only facilitates the discovery of novel drug candidates but also contributes to the development of more efficient and sustainable synthetic routes in pharmaceutical research and development.