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5,5-dimethyl-2-phenyl-1,3,2-dioxaphosphinane is a cyclic phosphorus-containing organic compound with the molecular formula C9H13O2P. It features a dioxaphosphinane ring structure, which consists of a phosphorus atom bonded to two oxygen atoms and a carbon atom, forming a three-membered ring. The molecule also contains two methyl groups (CH3) attached to the carbon atom adjacent to the phosphorus, and a phenyl group (C6H5) connected to the same carbon. 5,5-dimethyl-2-phenyl-1,3,2-dioxaphosphinane is known for its unique electronic properties and potential applications in various chemical reactions, such as a ligand in coordination chemistry or a building block in the synthesis of more complex phosphorus-containing molecules. Due to its stability and reactivity, it has been studied for its potential use in materials science and pharmaceuticals.

7526-31-0

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7526-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7526-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7526-31:
(6*7)+(5*5)+(4*2)+(3*6)+(2*3)+(1*1)=100
100 % 10 = 0
So 7526-31-0 is a valid CAS Registry Number.

7526-31-0SDS

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 5,5-Dimethyl-2-phenyl-1,3,2-dioxaphosphinane

1.2 Other means of identification

Product number -
Other names 2-phenyl-5,5-dimethyl-1,3,2-dioxaphosphorinane

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

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More Details:7526-31-0 SDS

7526-31-0Relevant academic research and scientific papers

Trimethylsilyl halide-promoted Michaelis-Arbuzov rearrangement

Renard, Pierre-Yves,Vayron, Philippe,Mioskowski, Charles

, p. 1661 - 1664 (2007/10/03)

(Matrix presented) We describe a new, straightforward, and easy-to-handle method for achieving an unprecedented trimethylsilyl halide-catalyzed Michaelis-Arbuzov-like rearrangement. This rearrangement occurs at temperatures from room temperature to 80°C and does not require addition of any alkyl halide. The scope and limitations of this new reaction are explored, as well as its mechanism.

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