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1,4-bis-dibutylphosphinoyl-butane, also known as bis(dibutylphosphino)butane, is a phosphorus-containing organic compound with the chemical formula C20H42P2. It is a white crystalline solid and is widely used as a ligand in homogeneous catalysis, particularly in transition metal complexes. This ligand is known for its ability to stabilize metal centers and enhance the catalytic activity of various reactions, such as hydrogenation, hydroformylation, and olefin polymerization. The structure of 1,4-bis-dibutylphosphinoyl-butane consists of a butane backbone with two dibutylphosphinoyl groups attached to the 1st and 4th carbon atoms, providing a flexible and sterically accessible environment for metal coordination. Its commercial availability and ease of synthesis make it a popular choice in the field of organometallic chemistry and catalysis.

4151-26-2

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4151-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4151-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4151-26:
(6*4)+(5*1)+(4*5)+(3*1)+(2*2)+(1*6)=62
62 % 10 = 2
So 4151-26-2 is a valid CAS Registry Number.

4151-26-2Downstream Products

4151-26-2Relevant academic research and scientific papers

A Simple Synthesis and Some Synthetic Applications of Substituted Phosphide and Phosphinite Anions

Tsvetkov, E. N.,Bondarenko, N. A.,Malakhova, I. G.,Kabachnik, M. I.

, p. 198 - 208 (2007/10/02)

Based on data for the acidity relationship of phosphines and phosphinous acids and water in dimethyl sulfoxide and water, a simple method is reported for the generation of phosphide and phosphinite anions by the action of concentrated aqueous alkali on primary and secondary phosphines as well as phosphinous acids in dimethyl sulfoxide or other dipolar aprotic solvents.Alkylation of the anion yields secondary and tertiary phosphines, polyphosphines, functionally substituted phosphines as well as similarly substituted phosphine oxides.Phosphinous acids have beenalkylated in various solvents in two-phase systems containing concentrated aqueous alkali and tetrabutylammonium iodide as phase transfer catalyst.

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