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(3R,9bS)-9b-Methyl-3-phenyl-2,3,5,9b-tetrahydro[1,3]oxazolo[2,3-a]isoindol-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

290332-71-7

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290332-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290332-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 290332-71:
(8*2)+(7*9)+(6*0)+(5*3)+(4*3)+(3*2)+(2*7)+(1*1)=127
127 % 10 = 7
So 290332-71-7 is a valid CAS Registry Number.

290332-71-7Relevant academic research and scientific papers

Meyers' bicyclic lactam formation under mild and highly stereoselective conditions

Penhoat, Ma?l,Leleu, Stephane,Dupas, Georges,Papamica?l, Cyril,Marsais, Francis,Levacher, Vincent

, p. 8385 - 8389 (2005)

New and mild conditions to prepare chiral bicyclic lactams in high yields and high diastereoselectivities are reported herein. This approach based on the activation of the carboxylic acid by means of Mukaiyama's reagent is an excellent alternative to Meye

Studies on the diastereoselective reductive alkylation of (R)-phenylglycinol derived phthalimide: Observation of stereoelectronic effects

Chen, Ming-De,He, Ming-Zhu,Zhou, Xiang,Huang, Li-Qiang,Ruan, Yuan-Ping,Huang, Pei-Qiang

, p. 1335 - 1344 (2007/10/03)

Full details of a flexible approach to N-protected (R)-3-alkyl-isoindolin- 1-ones 13 via diastereoselective reductive-alkylation are described, with emphasis on the stereochemical outcome of the key diastereoselective reactions. Additional experiments allowed finding remarkable stereoelectronic effects on the reductive ring-opening reactions.

Approaches to the synthesis of non-racemic 3-substituted isoindolinone derivatives

Allin, Steven M.,Northfield, Christopher J.,Page, Michael I.,Slawin, Alexandra M.Z.

, p. 1715 - 1721 (2007/10/03)

New methodology for the synthesis of non-racemic isoindolinone targets has been developed through application of tricyclic γ-lactam substrates as N-acyliminium ion precursors in reactions with carbon and hydride nucleophiles. Removal of the phenylglycinol

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