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(1-benzyl-allyl)-(2-phenyl-allyl)-carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

256950-53-5

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256950-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256950-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,9,5 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 256950-53:
(8*2)+(7*5)+(6*6)+(5*9)+(4*5)+(3*0)+(2*5)+(1*3)=165
165 % 10 = 5
So 256950-53-5 is a valid CAS Registry Number.

256950-53-5Downstream Products

256950-53-5Relevant academic research and scientific papers

(S)-Phenylalanine-derived chiral phosphorus-olefin ligands in rhodium-catalyzed asymmetric 1,4-addition reactions

Narui, Rintaro,Hayashi, Sayuri,Otomo, Haruka,Shintani, Ryo,Hayashi, Tamio

experimental part, p. 284 - 293 (2012/06/16)

Chiral phosphorus-olefins (S)-1, (S)-4, and (S)-5 have been designed and synthesized. These ligands were all synthesized from (S)-phenylalanine derivatives and act as phosphorus-olefin bidentate ligands to rhodium. The coordination face of the olefin can

Design and synthesis of new chiral phosphorus-olefin bidentate ligands and their use in the rhodium-catalyzed asymmetric addition of organoboroxines to N-sulfonyl imines

Shintani, Ryo,Narui, Rintaro,Tsutsumi, Yosuke,Hayashi, Sayuri,Hayashi, Tamio

supporting information; experimental part, p. 6123 - 6125 (2011/07/30)

Novel chiral phosphorus-olefin bidentate ligands have been synthesized in a few steps from a readily available enantiopure compound. These ligands have been applied to a rhodium-catalyzed asymmetric addition of organoboroxines to N-sulfonyl aldimines, achieving high yield and enantioselectivity.

Ring closing metathesis of phenyl-substituted dienes

Bujard,Briot,Gouverneur,Mioskowski

, p. 8785 - 8788 (2007/10/03)

A series of phenyl-substituted heterodienes 2a-f and 6 was prepared and subjected to ring closing metathesis (RCM) to give differently phenyl- substituted dihydropyrroles and dihydrofuran.

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