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1,3,2-Benzodioxaphosphole, 2-phenyl- is a complex organic compound with the molecular formula C9H7O2P. It is a derivative of benzodioxaphosphole, which is a heterocyclic compound containing a benzene ring, an oxygen atom, and a phosphorus atom. The 2-phenyl substitution refers to the presence of a phenyl group (C6H5) attached to the second carbon atom of the benzodioxaphosphole ring. see 1,3,2-Benzodioxaphosphole,2-phenyl- is of interest in organic chemistry and materials science due to its unique electronic properties and potential applications in the synthesis of various pharmaceuticals and agrochemicals. The structure and reactivity of 1,3,2-Benzodioxaphosphole, 2-phenyl- make it a valuable building block for the development of new compounds with specific properties and functions.

4759-37-9

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4759-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4759-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4759-37:
(6*4)+(5*7)+(4*5)+(3*9)+(2*3)+(1*7)=119
119 % 10 = 9
So 4759-37-9 is a valid CAS Registry Number.

4759-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,3,2-benzodioxaphosphole

1.2 Other means of identification

Product number -
Other names 2-phenyl-benzo[1,3,2]dioxaphosphole

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:4759-37-9 SDS

4759-37-9Relevant academic research and scientific papers

Reaction between Pyrocatechol and N,N,N',N'-Tetraethylphenylphosphonous Diamide

Kornilov,Roeva

, (2018)

The reaction between pyrocatechol and N,N,N',N'-tetraethylphenylphosphonous diamide was studied. It was found that the main reaction products are bisphosphorylated pyrocatehol and and the product of intramolecular cyclization, ester of pyrocatechol and ph

A new use of wittig-type reagents as 1,3-dipolar cycloaddition precursors and in pyrrole synthesis

St. Cyr, Daniel J.,Arndtsen, Bruce A.

, p. 12366 - 12367 (2007)

The one-pot reaction of imines, acid chlorides, and phosphonites has been found to generate a new class of phosphorus-based 1,3-dipolar cycloaddition reagent. These substrates, which are isomeric forms of classic Wittig reagents, undergo cycloaddition rea

Phospha-Muenchnones: Electronic structures and 1,3-dipolar cycloadditions

St-Cyr, Daniel J.,Morin, Marie S. T.,Belanger-Gariepy, Francine,Arndtsen, Bruce A.,Krenske, Elizabeth H.,Houk

experimental part, p. 4261 - 4273 (2010/08/06)

The reaction of imines, acid chlorides, PR3, and base generates a new class of 1,3-dipoles: phospha-Muenchnones. These 1,3-dipoles can undergo cycloadditions with alkynes followed by loss of phosphine oxides to form pyrroles. Cycloaddition reac

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