C98H88Cl5NP4Ru2
1783 g/mol
Research ReagentDanger
[1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane;dichlororuthenium;N-methylmethanamine;hydrochloride
CAS309735-86-2
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound
This compound is a ruthenium-based coordination complex used as a catalyst for asymmetric hydrogenation reactions. It features a chiral phosphine ligand framework, making it valuable in research settings for producing enantiomerically enriched compounds.
asymmetric hydrogenation catalyst
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
StrongSame Parent
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StrongSame Parent
Bis(acetato)[(1S)-[1,1'-binaphthalene]-2,2'-diylbis[bis(4-methylphenyl)phosphine]]ruthenium
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SimilarStructure SimilarSimilarity 0.75
Chloro[(S)-(-)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride
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SimilarStructure SimilarSimilarity 0.73
Dichloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium (II)
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SimilarStructure SimilarSimilarity 0.73
Chloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride
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ReferenceSame Category
BOC-alpha-Methylalanine
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Safety Reference
Danger
H228Flammable solid
Identifiers
IUPAC Name
bis([1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane);bis(dichlororuthenium);N-methylmethanamine;hydrochloride
InChIKey
FAAFCSOHMVBJIS-UHFFFAOYSA-J
SMILES
CC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=C(C=C7)C)C8=CC=C(C=C8)C.CC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=C(C=C7)C)C8=CC=C(C=C8)C.CNC.Cl.Cl[Ru]Cl.Cl[Ru]Cl
Synonyms (3)
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