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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)-

1,1'-Binaphthalene, 2,2'-dimethyl-

Cc1ccc2c(c1c1c(C)ccc3c1cccc3)cccc2 Request for Quotation
Chemical Name: 1,1'-Binaphthalene, 2,2'-dimethyl-
CAS Number: 32834-84-7
Product Number: AG00CV7S(AGN-PC-0JMS77)
Synonyms:
MDL No:
Molecular Formula: C22H18
Molecular Weight: 282.37832

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Chemical Structure


2,2'-Dimethyl-1,1'-binaphthalene, also known as DM-BINAP, is a versatile compound widely used in chemical synthesis as a chiral ligand in asymmetric catalysis. Its unique structure and chirality make it a highly effective tool in a variety of synthetic transformations, particularly in organometallic reactions. DM-BINAP is commonly employed in transition metal-catalyzed reactions to facilitate the formation of enantioselective products, making it an essential component in the production of pharmaceuticals, agrochemicals, and fine chemicals. This compound's ability to control the stereochemistry of reactions makes it an invaluable resource for chemists looking to produce optically pure compounds with high levels of efficiency and precision.