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Phosphine oxide, (3-methyl-1,2-butadienyl)diphenyl-, also known as 3-methyl-1,2-butadienyldiphenylphosphine oxide, is an organophosphorus compound with the chemical formula C15H15OP. It is a colorless to pale yellow liquid with a molecular weight of 242.26 g/mol. Phosphine oxide, (3-methyl-1,2-butadienyl)diphenyl- is characterized by the presence of a phosphorus atom bonded to two phenyl groups and a 3-methyl-1,2-butadienyl group. It is used as a ligand in coordination chemistry and as a reagent in organic synthesis, particularly in the formation of phosphorus-containing compounds. Due to its reactive nature, it is sensitive to air and moisture, and should be handled with care, typically under an inert atmosphere.

4145-83-9

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4145-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4145-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4145-83:
(6*4)+(5*1)+(4*4)+(3*5)+(2*8)+(1*3)=79
79 % 10 = 9
So 4145-83-9 is a valid CAS Registry Number.

4145-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylbuta-1,2-dien-1-yl)diphenylphosphine oxide

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

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More Details:4145-83-9 SDS

4145-83-9Relevant academic research and scientific papers

Convenient synthesis of allenylphosphoryl compounds: Via Cu-catalysed couplings of P(O)H compounds with propargyl acetates

Shen, Ruwei,Luo, Bing,Yang, Jianlin,Zhang, Lixiong,Han, Li-Biao

, p. 6451 - 6454 (2016/05/24)

A novel Cu-catalysed substitution reaction of propargyl acetates with P(O)H compounds is developed to afford allenylphosphoryl compounds via C-P bond coupling in high yields under mild conditions. A plausible mechanism involving the nucleophilic interception of the Cu-allenylidene intermediates is proposed.

Novel, stereoselective and stereospecific synthesis of allenylphosphonates and related compounds via palladium-catalyzed propargylic substitution

Kalek, Marcin,Stawinski, Jacek

supporting information; experimental part, p. 1741 - 1755 (2011/09/15)

We have developed a novel method for the synthesis of allenylphosphonates and related compounds based on a palladium(0)-catalyzed reaction of propargylic derivatives with H-phosphonate, H-phosphonothioate, H-phosphonoselenoate, and H-phosphinate esters. The reaction is stereoselective and stereospecific, and provides a convenient entry to a vast array of allenylphosphonates and their analogues with diverse substitution patterns in the allenic moiety and at the phosphorus center. Some mechanistic aspects of this new reaction were also investigated. Copyright

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