ChemicalBook >> CAS DataBase List >>(R)-(+)-TolBINAP

(R)-(+)-TolBINAP

CAS No.
99646-28-3
Chemical Name:
(R)-(+)-TolBINAP
Synonyms
(R)-TOL-BINAP;(R)-T-BINAP;(R)-(+)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL;(R)-(+)-2,2'98% (R)-TolBINAP;(R)-p-tolyl-BINAP;(R)-Tol-BINAP;(R)-(+)-2,2'-Bis(di-p-toL;phosphino)-1,1'-binaphthyL;Bis(diphenylphosphinyl)binaphthyl
CBNumber:
CB7334533
Molecular Formula:
C48H40P2
Molecular Weight:
678.8
MDL Number:
MFCD00269856
MOL File:
99646-28-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:11:07
Product description Number Pack Size Price
(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl 97% 668966 250mg $37.2
(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl 97% 668966 1g $134
(R)-(+)-TolBINAP >98.0%(HPLC) T3152 1g $72
(R)-(+)-TolBINAP >98.0%(HPLC) T3152 5g $216
(R)-(+)-2,2'-Bis(di-p-tolyl­phosphino)-1,1'-binaphthyl, 98% (R)-(+)-TolBINAP 98% 15-0152 250mg $30
More product size

(R)-(+)-TolBINAP Properties

Melting point 255-257 °C
alpha +156° (c 0.5, C6H6)
Boiling point 754.4±60.0 °C(Predicted)
storage temp. Inert atmosphere,Room Temperature
form Powder
color White to cream
optical activity [α]20/D +162°, c = 0.5 in benzene
Water Solubility Insoluble in water.
λmax 223nm(EtOH)(lit.)
InChIKey IOPQYDKQISFMJI-UHFFFAOYSA-N
SMILES P(C1C=CC(C)=CC=1)(C1C=CC(C)=CC=1)C1C=CC2=CC=CC=C2C=1C1C2=CC=CC=C2C=CC=1P(C1C=CC(C)=CC=1)C1C=CC(C)=CC=1
CAS DataBase Reference 99646-28-3(CAS DataBase Reference)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26
WGK Germany  3
TSCA  No
HS Code  29310099
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

(R)-(+)-TolBINAP price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 668966 (R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl 97% 99646-28-3 250mg $37.2 2023-06-20 Buy
Sigma-Aldrich 668966 (R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl 97% 99646-28-3 1g $134 2023-06-20 Buy
TCI Chemical T3152 (R)-(+)-TolBINAP >98.0%(HPLC) 99646-28-3 1g $72 2026-04-30 Buy
TCI Chemical T3152 (R)-(+)-TolBINAP >98.0%(HPLC) 99646-28-3 5g $216 2026-04-30 Buy
Strem Chemicals 15-0152 (R)-(+)-2,2'-Bis(di-p-tolyl­phosphino)-1,1'-binaphthyl, 98% (R)-(+)-TolBINAP 98% 99646-28-3 250mg $30 2026-04-30 Buy
Product number Packaging Price Buy
668966 250mg $37.2 Buy
668966 1g $134 Buy
T3152 1g $72 Buy
T3152 5g $216 Buy
15-0152 250mg $30 Buy

(R)-(+)-TolBINAP Chemical Properties,Uses,Production

Reaction

  1. Useful ligand for palladium-catalyzed carbon-oxygen bond formation.
  2. Ligand for palladium-catalyzed α-arylation of ketones.
  3. Ligand for Cu-catalyzed asymmetric conjugate reduction.
  4. Ligand for Cu-catalyzed asymmetric dienolate addition to aldehydes.
  5. Enantioselective conjugate reduction of lactones and lactams.
  6. Ligand used in the enantioselective cycloaddition of allenylsilanes with α-Imino esters.
  7. Catalytic Aldol reaction to ketones.
  8. Ligand with rhodium catalyses [2+2+2] cycloaddition reaction of alkenes and alkynes.
  9. Ligand used in the copper-catalyzed asymmetric conjugate addition of alkyl Grignard reagents on α,β-unsaturated esters.
  10. Ligand used in the copper-catalyzed asymmetric synthesis of cyclopropanes via tandem conjugate addition and intramolecular enolate trapping. 
Reactions of 99646-28-3_1
Reactions of 99646-28-3_2
Reactions of 99646-28-3_3

Chemical Properties

White to cream powder

Uses

(R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl is used as chiral catalyst ligand. (R)-T-BINAP complexes derived from rhodium precursors are used for the asymmetric hydroformylation of vinyl acetate. It is a catalysts used for reductive amination of ketones, Pt dications for cation trapping, Rh(I)-catalyst for hydrogenation of acetamidoacrylic acid derivatives.

Uses

(R)-T-BINAP complexes derived from rhodium precursors are used for the asymmetric hydroformylation of vinyl acetate. It may be employed as chiral catalyst for allylation of N-tosyl α-imino esters.

General Description

BINAP is based on a bis naphthalene backbone with different phosphine derivatives. 2,2′-bis(di-p-tolylphosphino)-1,1′-binaphthyl (p-Tol-BINAP)·AgF complex catalyzed asymmetric Mukaiyama-type aldol reaction is reported.

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
reaction type: Cross Couplings

Global( 156)Suppliers
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XINXIANG RUNYU MATERIAL CO., LTD.
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View Lastest Price from (R)-(+)-TolBINAP manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(R)-(+)-TolBINAP pictures 2026-07-09 (R)-(+)-TolBINAP
99646-28-3
1KG 98% 2000 Shenzhen Nexcon Pharmatechs Ltd.
(R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl pictures 2026-07-02 (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl
99646-28-3
$2.00-6.00 1kg 99% 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
(R)-(+)-TolBINAP pictures 2025-12-23 (R)-(+)-TolBINAP
99646-28-3
1kg 99% 200 XINXIANG RUNYU MATERIAL CO., LTD.
(R)-(+)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)1,1-BINAPHTHYL (R)-p-tolyl-BINAP (R)-(+)-2,2'-Bis(di-p-toL phosphino)-1,1'-binaphthyL (R)-(+)-2,2''-BIS(DI-P-TOLYLPHOSPHINO)-1,1''-BINAPHTHYL (R)-TOL-BINAP PHOSPHINE, 1,1''-(1R)-[1,1''-BINAPHTHALENE]-2,2''-DIYLBIS[BIS(4-METHYLPHENYL)- (R)-Tol-BINAP, (R)-(+)-2,2μ-Bis(di-p-tolylphosphino)-1,1μ-binaphthyl (R)-TolBINAP,99%e.e. 1,1'-(1R)-[1,1'-Binaphthalene]-2,2'-diylbis[bis(4-methylphenyl)phosphine] (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl, (R)-p-Tol-BINAP (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl,98%(R)-Tol-BINAP 98% (R)-TolBINAP (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl,98% (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl, 99% (R)-p-Tol-BINAP (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl 97% 1,1'-(1R)-[1,1'-Binaphthalene]-2,2'-diylbis[bis(4- methylphenyl)phosphine] (R)-(+)-2,2'-Bis-[bis-(p-tolylphosphino)]-1,1'-binaphthyl Phosphine, (1R)-[1,1'-binaphthalene]-2,2'-diylbis[bis(4-methylphenyl)- (r)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl, 95+% (R)-2,2’-Bis(di-p-tolylphosphino)-1,1’-binaphthalene (1R)-[1-[2-(bis-p-tolylphosphanyl)-1-naphthyl]-2-naphthyl]-bis(p-tolyl)phosphane 1,1'-(1R)-[1,1'-Binaphthalene]-2,2'-diylbis[bis(4-methylphenyl)phosphine 2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthalene (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl (R-tol-Binap) (R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl (R)-Tol-BINAP (R)-(+)-2,2' (R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl, CAS 99646-28-3 (r)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl, 95+% (R)-TOL-BINAP (R)-(+)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL (R)-T-BINAP Bis(diphenylphosphinyl)binaphthyl 99646-28-3 10165-88-6 C48H4OP2 Privileged Ligands Chiral Catalysts, Ligands, and Reagents BINAPs Asymmetric Synthesis Chiral Phosphine BINAP Series