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874221-90-6

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  • (11bR) -N- Methyl- N- [(S) - 1-Phenylethyl] - dinaphtho[2, 1- d:1', 2'- f] [1, 3, 2] dioxaphosphepin- 4- amine

    Cas No: 874221-90-6

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  • (11bR)?-N-?Methyl-?N-?[(S)?-?1-Phenylethyl]?-?dinaphtho[2,?1-?d:1',?2'-?f]?[1,?3,?2]?dioxaphosphepin-?4-?amine

    Cas No: 874221-90-6

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874221-90-6 Usage

General Description

R-N-Methyl-N-[(1S)-1-phenylethyl]-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-aMine is a complex compound with a long chemical name, often shortened to "R-Me-Phenyl-DPN" in research and industry. It is an organic molecule with a phosphorus atom in its structure, and it has potential applications in fields such as organic synthesis, pharmaceuticals, and materials science. R-N-Methyl-N-[(1S)-1-phenylethyl]-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-aMine may have interesting properties related to its molecular structure, and it could be used as a building block for the development of new materials or pharmacological compounds. However, further research and testing are necessary to fully understand its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 874221-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 874221-90:
(8*8)+(7*7)+(6*4)+(5*2)+(4*2)+(3*1)+(2*9)+(1*0)=176
176 % 10 = 6
So 874221-90-6 is a valid CAS Registry Number.

874221-90-6Downstream Products

874221-90-6Relevant articles and documents

Influence of phosphoramidites in copper-catalyzed conjugate borylation reaction

Sole, Cristina,Bonet, Amadeu,De Vries, Andre H. M.,De Vries, Johannes G.,Lefort, Laurent,Gulyas, Henrik,Fernandez, Elena

, p. 7855 - 7861 (2013/01/16)

Copper(I) has become the preferred metal to catalyze the β-boration of α,β-unsaturated carbonyl compounds, and now we demonstrate that easily accessible monodentate chiral ligands, such as phosphoramidites and phosphites, can be convenient alternative ligands to induce asymmetry in the enantioselective version of this reaction, particularly in the β-boration of α,β-unsaturated imines.

Efficient, selective, and green: Catalyst tuning for highly enatioselective reactions of ethylene

Smith, Craig R.,Rajanbabu

supporting information; experimental part, p. 1657 - 1659 (2009/04/10)

Fine tuning of the biaryl and amino moieties of Feringa's phosphoramidite ligands yields structurally simpler, yet more efficient and selective, ligands for asymmetric hydrovinylation of vinylarenes and acylic 1,3-dienes. The enantioselectivities and yields observed in the formation of the 3-arylbutenes are among the highest for all asymmetric catalytic processes reported to date for the synthesis of intermediates for the widely used antiinflammatory 2-arylpropionic acids including naproxen, ibuprofen, fenoprofen, and flurbiprofen.

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