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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)-

Oligomycin A, 21-hydroxy-

CC[C@H]1/C=C/C=C/C[C@@H](C)[C@H](O)[C@@](C)(O)C(=O)[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@H]([C@@H]([C@H](/C=C/C(=O)O[C@@H]2[C@@H]([C@H](C[C@H]1O)O[C@]1(CC[C@@H]([C@@H](O1)C[C@H](O)C)C)[C@H]2C)C)C)O)C Request for Quotation
Chemical Name: Oligomycin A, 21-hydroxy-
CAS Number: 102042-09-1
Product Number: AG008SON(AGN-PC-0OR5Z9)
Synonyms:
MDL No: MFCD09752734
Molecular Formula: C45H74O12
Molecular Weight: 807.0619

Identification/Properties

Computed Properties
Molecular Weight:
807.075g/mol
XLogP3:
5.9
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
3
Exact Mass:
806.518g/mol
Monoisotopic Mass:
806.518g/mol
Topological Polar Surface Area:
200A^2
Heavy Atom Count:
57
Formal Charge:
0
Complexity:
1430
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
18
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
3
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


21-Hydroxyoligomycin A is a highly versatile compound, which finds significant application in chemical synthesis as a key building block for creating diverse molecular structures. This compound's unique chemical properties make it a valuable asset in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and materials science. Its hydroxy group provides a reactive site for various functionalization reactions, enabling the synthesis of complex molecules with precision and efficiency. By utilizing 21-Hydroxyoligomycin A as a starting material or intermediate, chemists can access a wide range of structural derivatives that exhibit tailored properties and functions, making it an indispensable tool in modern synthetic chemistry.