Welcome to LookChem.com Sign In|Join Free
  • or
Diphenyl(2-phenylethenyl)phosphane sulfide, also known as diphenyl(2-phenylethenyl)phosphine sulfide, is an organophosphorus compound with the chemical formula C18H15PS. It is a colorless to pale yellow solid, soluble in organic solvents, and has a molecular weight of 294.35 g/mol. diphenyl(2-phenylethenyl)phosphane sulfide is characterized by the presence of a phosphorus atom bonded to two phenyl groups and a 2-phenylethenyl group, with a sulfur atom attached to the phosphorus atom. It is used in various applications, including as a ligand in coordination chemistry, a reagent in organic synthesis, and a precursor in the preparation of other organophosphorus compounds. Due to its potential reactivity and toxicity, it should be handled with care and used in accordance with proper safety protocols.

4319-11-3

Post Buying Request

4319-11-3 Suppliers

Recommended suppliers

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

4319-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4319-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4319-11:
(6*4)+(5*3)+(4*1)+(3*9)+(2*1)+(1*1)=73
73 % 10 = 3
So 4319-11-3 is a valid CAS Registry Number.

4319-11-3SDS

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 diphenyl-(2-phenylethenyl)-sulfanylidene-$l^{5}-phosphane

1.2 Other means of identification

Product number -
Other names 1,3-Diphenyl-disiloxan

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:4319-11-3 SDS

4319-11-3Relevant academic research and scientific papers

Rapid Synthesis of Chiral 1,2-Bisphosphine Derivatives through Copper(I)-Catalyzed Asymmetric Conjugate Hydrophosphination

Xiao, Jun-Zhao,Yin, Liang,Yue, Wen-Jun,Zhang, Shuai

, p. 7057 - 7062 (2020/03/23)

1,2-Bisphosphines have been identified as one class of important and powerful chiral ligands in asymmetric catalysis with transition metals. Herein, a copper(I)-catalyzed asymmetric hydrophosphination of α,β-unsaturated phosphine sulfides was developed wi

Vic-Diphosphination of Alkenes with Silylphosphine under Visible-Light-Promoted Photoredox Catalysis

Otomura, Nobutaka,Okugawa, Yuto,Hirano, Koji,Miura, Masahiro

supporting information, p. 4802 - 4805 (2017/09/23)

An Ir(ppy)3-catalyzed vic-diphosphination of styrenes with Me3Si-PPh2 and NFSI proceeds under blue LED irradiation to afford the corresponding bis(diphenylphosphino)ethane derivatives without any formation of hydrophosphination byproducts, which are inevitable and problematic under the previous Cu/NHC catalysis. Additionally, the visible-light-promoted photoredox catalysis enables the diphosphination of relatively challenging aliphatic alkenes and β-substituted styrene.

Radical addition reactions of diphenylphosphine sulfide

Parsons, Andrew F.,Sharpe, David J.,Taylor, Philip

, p. 2981 - 2983 (2007/10/03)

Radical additions of diphenylphosphine sulfide [Ph2P(S)H] to various C=C bonds offers a general, mild and efficient approach to alkyl(diphenyl)phosphine sulfides. Georg Thieme Verlag Stuttgart.

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 4319-11-3