Welcome to LookChem.com Sign In|Join Free
  • or
Dinaphthalen-1-yl(phenyl)phosphane, also known as 1,1'-binaphthalen-2-yl-2-phenylphosphane, is an organophosphorus compound characterized by a binaphthalene core with a phenyl group attached to a phosphorus atom. This molecule is of interest in the field of asymmetric catalysis, particularly in the development of chiral ligands for transition metal catalysts. The binaphthalene framework provides a rigid, chiral environment that can influence the selectivity of reactions, making it a valuable component in the design of catalysts for enantioselective synthesis. The phenyl group further modulates the electronic properties and steric interactions of the ligand, which can be tailored for specific applications. dinaphthalen-1-yl(phenyl)phosphane is a testament to the importance of molecular structure in dictating chemical reactivity and selectivity in synthetic chemistry.

3135-67-9

Post Buying Request

3135-67-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3135-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3135-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3135-67:
(6*3)+(5*1)+(4*3)+(3*5)+(2*6)+(1*7)=69
69 % 10 = 9
So 3135-67-9 is a valid CAS Registry Number.

3135-67-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dinaphthalen-1-yl(phenyl)phosphane

1.2 Other means of identification

Product number -
Other names Phosphine,di-1-naphthalenylphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3135-67-9 SDS

3135-67-9Relevant academic research and scientific papers

Rhodium catalyzed hydroformylation assisted by cyclodextrins in biphasic medium: Can sulfonated naphthylphosphanes lead to active, selective and recyclable catalytic species?

Elard, Maxime,Denis, Julien,Ferreira, Michel,Bricout, Hervé,Landy, David,Tilloy, Sébastien,Monflier, Eric

, p. 47 - 54 (2015/03/30)

New sulfonated naphthylphosphanes having an average sulfonation degree around 2 have been synthetized and tested as ligand in the aqueous biphasic Rh-catalyzed hydroformylation of 1-decene assisted by randomly methylated β-cyclodextrins. All these water-soluble phosphanes associated to a rhodium precursor were able to perform aqueous hydroformylation of 1-decene. The best results in terms of catalyst recovery and recycling were obtained with sulfonated 2-naphthylphosphanes. With sulfonated 1-naphthylphosphanes, formation of low-coordinated catalytic species leading to a catalyst leaching in the organic phase was postulated. These results were rationalized by considering that sulfonated 1-naphthylphosphanes are bulkier ligands than sulfonated 2-naphthylphosphanes.

SYNTHESIS AND MOLECULAR STRUCTURES OF FLUOROPHOSPHORANES, R3PF2, ISOELECTRONIC WITH ANIONIC FLUOROSILICATES

Holmes, Robert R.,Holmes, Joan M.,Day, Roberta O.,Swamy, K. C. Kumara,Chandrasekhar, V.

, p. 153 - 170 (2007/10/02)

The new difluorophosphoranes Ph(o-Tol)2PF2 (1), Mes3PF2 (2), Ph(1-Np)2PF2 (3), (o-Tol)3PF2, (p-Tol)3PF2, Ph(t-Bu)2PF2, and (Ph2PF2)2CH2 containing bulky substituents were prepared by the fluorination reaction of precursor organophosphines with dimethylaminosulfur trifluoride.They were characterized by 1H, 31P, and 19F NMR spectra.The molecular structures of 1-3 revealed trigonal bipyramidal geometries.Comparison of the structural data with that of isoelectronic anionic fluorosilicates along with the NMR data suggest the operation of a steric effect that increases bond lengths in the difluorophosphoranes 1-3 and in related anionic silicates.The data are discussed relative to enhanced reactivity observed for anionic silicates. 1 cryatallizes in the monoclinic space group C2/c with a = 11.819(3) Angstroem, b = 10.163(2) Angstroem, c = 13.992 Angstroem, β = 99.14(2) deg, and Z = 4. 2 crystallizes in the monoclonic space group C2/c with a = 10.531(2) Angstroem, b = 12.667(2) Angstroem, c = 18.110(4) Angstroem, β = 104.21(2) deg, and Z = 4. 3 crystallizes in the monoclinic space group P21/c with a = 15.868(2) Angstroem, b = 7.434(1) Angstroem, c = 18.213(4) Angstroem, β = 112.34(2) deg, and Z = 4.The final conventional unweighted residuals are 0.063 (1), 0.060 (2), and 0.040 (3).Key words: Difluorophosphoranes, anionic fluorosilicates, x-ray structures, NMR spectra

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3135-67-9