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N-(8-mentholyl)-(3aS,6S,7aS)-6-ethyl-3a,6,7,7a-tetrahydroisoindoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

237058-22-9

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237058-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237058-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,0,5 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 237058-22:
(8*2)+(7*3)+(6*7)+(5*0)+(4*5)+(3*8)+(2*2)+(1*2)=129
129 % 10 = 9
So 237058-22-9 is a valid CAS Registry Number.

237058-22-9Downstream Products

237058-22-9Relevant academic research and scientific papers

Thermal and Lewis acid catalyzed diastereoselective intramolecular Diels-Alder reaction on α,β-unsaturated amides derived from (-)-8- aminomenthol

Andres, Celia,Garcia-Valverde, Maria,Nieto, Javier,Pedrosa, Rafael

, p. 5230 - 5236 (2007/10/03)

Stereochemical aspects of the intramolecular Diels-Alder reaction on perhydro-1,3-benzoxazines derived from (-)-8-aminomenthol bearing α,β- unsaturated amides and the dienic component attached at C-2 are described. The thermal cyclization of 2-(2'-furyl) derivatives 2, 6, and 7 exclusively afforded mixtures of exo adducts. The product selectivity was highly dependent on the solvent of the reaction. In CH2Cl2, the kinetic products 3, 8, and 9 always predominated, whereas in hexane or toluene, less polar solvents, the thermodynamic adducts 4, 10, and 11 were formed as major diastereoisomers. In cyclizations catalyzed with equimolar or 2-fold excess of Lewis acid, the kinetic stereiosomers were predominant. Some Lewis acids catalyzed the reaction, but diethylaluminum chloride was the most effective. The cyclization on the perhydro-1,3-benzoxazine 13, bearing an open dienic component, was much less stereoselective, and a mixture of two exo and two endo possible stereoisomers were formed. Elimination of the menthol appendage in two steps by reductive ring opening of the N,O-acetal moiety and oxidation-elimination yielded enantiomerically pure tetrahydroisoindoline derivatives.

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