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diethyl (2,3-dimethylphenyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72596-34-0

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72596-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72596-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,9 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72596-34:
(7*7)+(6*2)+(5*5)+(4*9)+(3*6)+(2*3)+(1*4)=150
150 % 10 = 0
So 72596-34-0 is a valid CAS Registry Number.

72596-34-0Relevant academic research and scientific papers

Manganese(III)-mediated direct phosphonylation of arenes

Xu, Wei,Zou, Jian-Ping,Zhang, Wei

experimental part, p. 2639 - 2643 (2010/06/16)

Manganese (III)-promoted direct phosphonylation of mono- and disubstituted arenes with dialkylphosphite afforded regioselective dialkylphosphonates in good yields. The reactions can apply to arenes bearing electron-donating groups and electron-withdrawing

Naphthalocyanine compound and production thereof

-

, (2008/06/13)

Disclosed is a novel naphthalocyanine compound which strongly absorbs light or near infrared region and which is chemically stable and highly soluble to an organic solvent. The naphthalocyanine compound is represented by the following formula [1]; STR1 wh

Oxidative Phoshonylation of Aromatics with Ammonium Cerium(IV) Nitrate

Kottmann, Hariolf,Skarzewski, Jacek,Effenberger, Franz

, p. 797 - 801 (2007/10/02)

Arylphosphonates 5 and 6 can be prepared in good yields in a one-step synthesis starting from arenes with tri- or diethylphosphites and cerium ammonium nitrate (CAN) as oxidant.The seletivity of the oxidative phosphonylation is relatively low; the reactive species is a phosphite radical cation.

OXIDATIVE PHOSPHONYLATION OF AROMATIC COMPOUNDS

Effenberger, Franz,Kottmann, Hariolf

, p. 4171 - 4182 (2007/10/02)

Aryl phosphonates can be prepared in good yield from the respective arenes and tri- or dialkylphosphites by either chemical or anodic oxidation.The anodic oxidation proceeds either via phosphinium radical cations, which then attack the arenes electrophilically, or via arene radical cations, which add the trialkylphosphite as nucleophile.Aryl phosphonates are also obtained in good yield by chemical oxidation with peroxodisulfate/AgNO3 in acetonitrile/water or glacial acetic acid.The diethylphosphinium radical cation, formed from diethylphosphite by oxidation with Ag(II), is supposed to be the reactive species in this process.Raising the silver salt concentration leads to an increase in polyphosphonylation.Selectivity ratios were determined for the oxidative phosphonylation process.

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