C52H48P2
734.9 g/mol
Research ReagentWarning
(R)-(+)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL
CAS135139-00-3EC681-146-8
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound
This compound is a sterically demanding bidentate phosphine ligand, specifically designed for use in asymmetric catalysis. Its significance lies in its role as a chiral ligand that can induce high enantioselectivity in transition-metal-catalyzed reactions, making it a standard tool in organic synthesis research.
chiral ligand for asymmetric hydrogenationligand for enantioselective cross-coupling 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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CAS 135139-00-3
Related Compounds
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(R)-(+)-2,2'-Bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl
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(R)-(+)-2,2'-Bis(diphenylphospino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl
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research compound
ApplicationSame Use
(S)-(-)-2,2'-Bis(diphenylphospino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl
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ReferenceSame Category
1-(4-Methoxybenzyl)-1,5,6,7-tetrahydro-4H-indazol-4-one
CAS1352907-89-1
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Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane
InChIKey
MXGXXBYVDMVJAO-UHFFFAOYSA-N
SMILES
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
Synonyms (30)
- DM-BINAP
- (R)-(+)-XYLBINAP
- (R)-3,5-XYLYL-BINAP
- (R)-DM-BINAP
- (S)-(-)-XYLBINAP
- (S)-DM-BINAP
- 3,5-Xylyl-BINAP