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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)-

Kryptand 222B

C1COCCN2CCOCCOCCN(CCO1)CCOc1c(OCC2)cccc1 Request for Quotation
Chemical Name: Kryptand 222B
CAS Number: 31250-18-7
Product Number: AG007I2O(AGN-PC-0JSNG0)
Synonyms:
MDL No: MFCD00013324
Molecular Formula: C22H36N2O6
Molecular Weight: 424.5310

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Chemical Structure


The versatile compound Kryptofix 222B is a highly effective phase-transfer catalyst commonly used in chemical synthesis processes. Its unique molecular structure allows it to facilitate the transfer of a wide range of organic and inorganic ions between immiscible phases, making it an essential tool in various reactions.Kryptofix 222B is particularly valued for its ability to activate nucleophiles, such as halides, while inhibiting unwanted side reactions. This property makes it ideal for promoting substitution and addition reactions, especially in alkaline conditions where other catalysts may fail.In addition, Kryptofix 222B has found significant utility in the preparation of various pharmaceutical intermediates, agrochemicals, and functional materials. Its high efficiency and selectivity make it a preferred catalyst in the synthesis of complex organic molecules.Overall, Kryptofix 222B plays a crucial role in enhancing the efficiency and selectivity of chemical syntheses, making it a valuable tool for researchers and chemists in a wide range of applications.