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Home/Compounds/Research Reagent/[Rh COD (R)-Binap]BF4
C52H44BF4P2Rh
920.6 g/mol
Research Reagent

[Rh COD (R)-Binap]BF4

CAS208118-82-5
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound

This compound is a rhodium-based chiral hydrogenation catalyst featuring a (R)-BINAP ligand and cyclooctadiene, supplied as a tetrafluoroborate salt for research applications.

Chiral hydrogenation catalyst in asymmetric synthesisResearch reagent for enantioselective reactions

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

StrongStructure SimilarSimilarity 1.00

Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II)

CAS325146-81-4

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StrongStructure SimilarSimilarity 1.00

[Rh COD (R)-Binap]BF4

CAS439801-50-0

research compound

StrongStructure SimilarSimilarity 1.00

(+)-BINAP

CAS76189-55-4

research compound

StrongStructure SimilarSimilarity 1.00

(-)-BINAP

CAS76189-56-5

research compound

ApplicationSame Use

Diacetato[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II)

CAS261948-85-0

research compound

ApplicationSame Use

PUBCHEM_71310552

CAS944450-44-6

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ApplicationSame Use

Ru(OAc)2[(R)-dtbm-segphos]

CAS1025477-38-6

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ReferenceSame Category

5-Bromonicotinic acid

CAS20826-04-4

research compound

Identifiers
IUPAC Name

(1Z,5Z)-cycloocta-1,5-diene;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane;rhodium;tetrafluoroborate

InChIKey

NXRNGSUCQWUDOA-ONEVTFJLSA-N

SMILES

[B-](F)(F)(F)F.C1/C=C\CC/C=C\C1.C1=CC=C(C=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C45)P(C6=CC=CC=C6)C7=CC=CC=C7)C8=CC=CC=C8.[Rh]

Synonyms (5)
  • [Rh COD (R)-Binap]BF4
  • [Rh COD (S)-Binap]BF4
  • [Rh COD (S)-Binap]BF4, Rh
  • [Rh COD (rac)-Binap]BF4

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