Welcome to LookChem.com Sign In|Join Free
  • or
Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is a lithium salt of a phosphine compound, characterized by its white to off-white solid appearance and solubility in various organic solvents. It is widely recognized for its role as a ligand in coordination and organometallic chemistry, and is particularly noted for its catalytic properties in organic reactions, especially in the formation of carbon-carbon and carbon-heteroatom bonds.

113330-71-5

Post Buying Request

113330-71-5 Suppliers

Recommended suppliers

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

113330-71-5 Usage

Uses

Used in Catalysts for Organic Reactions:
Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is used as a catalyst for facilitating the formation of carbon-carbon and carbon-heteroatom bonds in organic reactions. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to form stable complexes with metal ions aids in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is utilized in the agrochemical industry for the synthesis of pesticides and other agrochemicals. Its catalytic properties contribute to the production of more effective and environmentally friendly products.
Used in Material Science:
In the field of material science, Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is used in the development of new materials with unique properties. Its ability to form stable complexes with various metal ions makes it a promising candidate for the creation of advanced materials with applications in electronics, energy storage, and other areas.
Used in Research Laboratories:
As a reagent in research laboratories, Phosphine, diphenyl[2-(phenylphosphino)ethyl]-, lithium salt is employed for its versatility in various chemical reactions and its potential to yield novel compounds and materials. Its use in academic and industrial research settings contributes to the advancement of chemical knowledge and the discovery of new applications.

Check Digit Verification of cas no

The CAS Registry Mumber 113330-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113330-71:
(8*1)+(7*1)+(6*3)+(5*3)+(4*3)+(3*0)+(2*7)+(1*1)=75
75 % 10 = 5
So 113330-71-5 is a valid CAS Registry Number.

113330-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name lithium (2-(diphenylphosphino)ethyl)(phenyl)phosphanide

1.2 Other means of identification

Product number -
Other names -

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:113330-71-5 SDS

113330-71-5Downstream Products

113330-71-5Relevant academic research and scientific papers

THE CLEAVAGE OF P-C BONDS IN DIPHOSPHINES BY LITHIUM: THE CRYSTAL STRUCTURE OF 2(OC4H8)8>

Brooks, Peter,Craig, Donald C.,Gallagher, Michael J.,Rae, A. David,Sarrof, Adrien

, p. C1 - C4 (2007/10/02)

Reaction of alkane-1,n-diylbisdiphenylphosphines with lithium in tetrahydrofuran gives only the diphosphides resulting from cleavage of a phosphorus-aryl bond at each end of the chain; the course of the reaction is independent of chain length.The X-ray structure of the ethane diphosphide is presented and a possible mechanism discussed.

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 113330-71-5