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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)-

Cyclosporin U

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Chemical Name: Cyclosporin U
CAS Number: 108027-45-8
Product Number: AG008XJU(AGN-PC-0OXYSL)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Cyclosporin U, an intriguing compound derived from the fungus Tolypocladium inflatum, finds significant utility in the realm of chemical synthesis. This unique molecule serves as a valuable tool for chemists seeking to embark on intricate organic transformations and novel synthetic routes. Leveraging the distinct structure and reactivity of Cyclosporin U, researchers can exploit its functional groups and chiral centers to facilitate the construction of complex molecular architectures with high precision and efficiency. From serving as a versatile building block to catalyzing key reactions, Cyclosporin U holds immense potential in enabling the synthesis of a diverse array of compounds with diverse applications in pharmaceuticals, materials science, and beyond.