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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)-

Phorbol-12,13-didecanoate

CCCCCCCCCC(=O)OC1CC2C(C3C1(OC=O)C3(C)C)C=C(CC1(C2C=C(C1=O)C)O)CO Request for Quotation
Chemical Name: Phorbol-12,13-didecanoate
CAS Number: 24928-17-4
Product Number: AG007OIB(AGN-PC-00URZQ)
Synonyms:
MDL No: MFCD00065449
Molecular Formula: C30H44O7
Molecular Weight: 516.6662

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Chemical Structure


Phorbol 12,13-didecanoate, a derivative of phorbol ester, serves as a valuable reagent in chemical synthesis by virtue of its unique chemical properties. This compound's structural characteristics make it particularly suited for use as a catalyst or building block in various organic reactions. In organic synthesis, Phorbol 12,13-didecanoate is commonly employed in esterification and transesterification reactions to form ester bonds, a fundamental step in the construction of complex organic molecules. Additionally, it can act as a Lewis acid catalyst in certain transformations, facilitating the conversion of functional groups and promoting desired chemical reactions. Overall, the versatile nature of Phorbol 12,13-didecanoate makes it an essential tool for chemists engaged in the synthesis of novel compounds and materials.