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diisopropyl (4-methoxybenzyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34586-54-4

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34586-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34586-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,8 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34586-54:
(7*3)+(6*4)+(5*5)+(4*8)+(3*6)+(2*5)+(1*4)=134
134 % 10 = 4
So 34586-54-4 is a valid CAS Registry Number.

34586-54-4Relevant academic research and scientific papers

Visible-light-mediated phosphonylation reaction: formation of phosphonates from alkyl/arylhydrazines and trialkylphosphites using zinc phthalocyanine

Hosseini-Sarvari, Mona,Koohgard, Mehdi

, p. 5905 - 5911 (2021/07/12)

In this work, we developed a ligand- and base-free visible-light-mediated protocol for the photoredox syntheses of arylphosphonates and, for the first time, alkyl phosphonates. Zinc phthalocyanine-photocatalyzed Csp2-P and Csp3-P bond formations were efficiently achieved by reacting aryl/alkylhydrazines with trialkylphosphites in the presence of air serving as an abundant oxidant. The reaction conditions tolerated a wide variety of functional groups.

Palladium-catalyzed α-arylation of benzylic phosphonates

Montel, Sonia,Raffier, Ludovic,He, Yuying,Walsh, Patrick J.

supporting information, p. 1446 - 1449 (2014/04/03)

A new synthetic route to access diarylmethyl phosphonates is presented. The transformation enables the introduction of aromatic groups on benzylic phosphonates via a deprotonative cross-coupling process (DCCP). The Pd(OAc) 2/CataCXium A-based catalyst afforded a reaction between benzyl diisopropyl phosphonate derivatives and aryl bromides in good to excellent isolated yields (64-92%).

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