(S)-(-)-TolBINAP CAS 100165-88-6 Purity >98.0% (HPLC)

Short Description:

(S)-(-)-2,2′-Bis(di-p-Tolylphosphino)-1,1′-Binaphthyl

Synonyms: (S)-(-)-TolBINAP 

CAS: 100165-88-6

Purity: >98.0% (HPLC)

Appearance: White to Off-White Powder 

Contact: Dr. Alvin Huang

Mobile/Wechat/WhatsApp: +86-15026746401

E-Mail: alvin@ruifuchem.com


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100165-88-6 - Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer of (S)-(-)-TolBINAP (CAS: 100165-88-6) with high quality. Ruifu Chemical can provide worldwide delivery, competitive price, excellent service, small and bulk quantities available. Purchase (S)-(-)-TolBINAP, Please contact: alvin@ruifuchem.com

100165-88-6 - Chemical Properties:

Chemical Name (S)-(-)-2,2'-Bis(di-p-Tolylphosphino)-1,1'-Binaphthyl 
Synonyms (S)-(-)-TolBINAP (S)-Tol-BINAP; (S)-T-BINAP; (S)-Tol-BINA; (-)-Tol-BINA; (-)-Tol-BINAP
Stock Status In Stock, Commercial Production  
CAS Number 100165-88-6 
Molecular Formula C48H40P2
Molecular Weight 678.80 g/mol
Melting Point 252.0~259.0℃ 
Sensitive Air Sensitive. Store Under Inert Gas
Water Solubility  Insoluble in Water 
COA & MSDS Available
Product Categories  Ligands; Chiral Ligands
Origin Shanghai, China
Brand Ruifu Chemical

100165-88-6 - Specifications:

Items Specifications Results
Appearance White to Off-White Powder  White Powder            
Melting Point 252.0~259.0℃ 256.9℃
Purity / Analysis Method >98.0% (HPLC)  98.5% 
Purity / Analysis Method 97.5~102.5% (Neutralization Titration)  Complies
Optical Purity (e.e)   >99.0% (HPLC)  99.2%
Specific Rotation [a]20/D -167.0°~-157.0° (C=1.052, Benzene) -158.7°
Infrared Spectrometry  Consistent with Structure Complies
1H NMR Spectrum Consistent with Structure Complies
Conclusion The product has been tested and complies with the given specifications

Package/Storage/Shipping:

Package: Fluorinated Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement.
Storage Condition: Keep the container tightly closed and store in a cool, dry and well-ventilated warehouse away from incompatible substances. Protect from light and moisture.
Shipping: Deliver to worldwide by air, by FedEx / DHL Express. Provide fast and reliable delivery. 

Advantages:

Sufficient Capacity: Sufficient facilities and technicians

Professional Service: One stop purchasing service

OEM Package: Custom package and label available

Fast Delivery: If within stock, three days delivery guaranteed

Stable Supply: Maintain reasonable stock    

Technical Support: Technology solution available

Custom Synthesis Service: Ranged from grams to kilos

High Quality: Established a complete quality assurance system

FAQ:

How to Purchase? Please contact Dr. Alvin Huang: sales@ruifuchem.com or alvin@ruifuchem.com 

15 Years Experience? We have more than 15 years of experience in the manufacture and export of a wide range of high quality pharmaceutical intermediates or fine chemicals.

Main Markets? Sell to domestic market, North America, Europe, India, Korea, Japanese, Australia, etc.

Advantages? Superior quality, affordable price, professional services and technical support, fast delivery.

Quality AssuranceStrict quality control system. Professional equipment for analysis include NMR, LC-MS, GC, HPLC, ICP-MS, UV, IR, OR, K.F, ROI, LOD, MP, Clarity, Solubility, Microbial limit test, etc.

SamplesMost products provide free samples for quality evaluation, shipping cost should be paid by customers.

Factory AuditFactory audit welcome. Please make an appointment in advance.

MOQ? No MOQ. Small order is acceptable.

Delivery Time? If within stock, three days delivery guaranteed.

TransportationBy Express (FedEx, DHL), by Air, by Sea.

Documents? After sales service: COA, MOA, ROS, MSDS, etc. can be provided.

Custom SynthesisCan provide custom synthesis services to best fit your research needs.

Payment TermsProforma invoice will be sent first after confirmation of order, enclosed our bank information. Payment by T/T (Telex Transfer), PayPal, Western Union, etc. 

100165-88-6 - Risk and Safety:

Risk Codes
36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany 3
TSCA No
HS Code 2931900090

100165-88-6 - Reaction:

(S)-(-)-2,2'-Bis(di-p-Tolylphosphino)-1,1'-Binaphthyl ((S)-(-)-TolBINAP) (CAS: 100165-88-6) Reaction
Useful ligand for palladium-catalyzed carbon-oxygen bond formation.
Ligand for palladium-catalyzed α-arylation of ketones.
Ligand for Cu-catalyzed asymmetric conjugate reduction.
Ligand for Cu-catalyzed asymmetric dienolate addition to aldehydes.
Enantioselective conjugate reduction of lactones and lactams.
Ligand used in the enantioselective cycloaddition of allenylsilanes with α-Imino esters.
Catalytic Aldol reaction to ketones.
Ligand with rhodium catalyses [2+2+2] cycloaddition reaction of alkenes and alkynes.
Ligand used in the iridium-catalyzed enantioselective C-H bond activation of 2-(alkylamino)-pyridine with alkenes.
Iridium-catalyzed regio-, diastereo-, and enantioselective tert-(hydroxyl)-prenylation of alcohols.
Rhodium-catalyzed cross cyclotrimerization.

100165-88-6 - Application:

(S)-(-)-2,2'-Bis(di-p-Tolylphosphino)-1,1'-Binaphthyl ((S)-(-)-TolBINAP) (CAS: 100165-88-6) is chiral ligand widely used in asymmetric synthesis. It also used as excellent catalysts for asymmetric hydrogenation of alkenes and some cyclic anhydrides. BINAP is used in organic synthesis for enantioselective transformations catalyzed by its complexes of ruthenium, rhodium, and palladium.
(S)-(-)-TolBINAP reacts with silver nitrate to form (S)-Tol-BINAP·AgNO3, which can catalyze the enantioselective allylation reaction of aldehydes to form enantiopure secondary alcohols. It may be used as a chiral ligand in the palladium catalyzed asymmetric double carbohydroamination of iodoarenes to form α-aminoamides. It can also catalyze the asymmetric N-allylation reaction of ortho-tert-butylanilide derivatives with diallyl carbonate to form chiral N-allyl ortho-tert-butylanilides. 

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