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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)-

Icodextrin

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Chemical Name: Icodextrin
CAS Number: 337376-15-5
Product Number: AG0037O4(AGN-PC-0R99LT)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The application of Icodextrin in chemical synthesis involves its use as a versatile and efficient reagent for various reactions. Icodextrin, a type of cyclic dextrin, possesses a unique structure with a hydrophobic cavity that can encapsulate guest molecules. This property allows Icodextrin to act as a host molecule in host-guest chemistry, providing a controlled environment for chemical reactions to take place. In addition, Icodextrin is known for its chiral recognition capabilities, making it a valuable tool in asymmetric synthesis. Its ability to selectively bind to specific enantiomers can lead to the formation of enantiopure compounds, essential in the pharmaceutical and agrochemical industries. Furthermore, Icodextrin can serve as a phase-transfer catalyst, facilitating reactions between immiscible reactants by transferring ions or molecules between different phases. Overall, the unique properties of Icodextrin make it a versatile and valuable component in various chemical synthesis processes.