This compound is a ruthenium complex coordinated with two acetic acid molecules and a chiral bisphosphine ligand featuring multiple 3,5-dimethylphenyl substituents. It is employed as a chiral catalyst for asymmetric synthesis, primarily in research settings.
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Diacetato{(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II)
asymmetric hydrogenation catalyst
[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;N-methylmethanamine;ruthenium;trichloronioruthenium(1-);chloride;hydrochloride
asymmetric hydrogenation catalyst
Chloro[(S)-2,2'-bis(bis(3,5-dimethylphenyl)phosphino)-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride
asymmetric hydrogenation catalyst
Chloro[(S)-2,2'-bis(bis(3,5-dimethylphenyl)phosphino)-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride
asymmetric hydrogenation catalyst
(S)-Ru(OAc)2(H8-BINAP)
asymmetric hydrogenation catalyst
Tris(4-methylphenyl)sulfanium bromide
Research reagent
2-(Methoxycarbonyl)benzeneboronic Acid
Suzuki coupling reagent
Nbi 31772
insulin-like growth factor binding protein inhibitor
acetic acid;[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;ruthenium
HDUAMHMUQGCXCT-UHFFFAOYSA-N
CC1=CC(=CC(=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(=O)O.CC(=O)O.[Ru]
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