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(1S,3R,5S,5aS,7aS,7bR)-octahydro-1-(4-methoxybenzyloxy)-1-methyl-3-benzyl-5-methyl-7b-methylcyclopenta[gh]pyrrolizinium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1304686-93-8

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1304686-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304686-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,6,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1304686-93:
(9*1)+(8*3)+(7*0)+(6*4)+(5*6)+(4*8)+(3*6)+(2*9)+(1*3)=158
158 % 10 = 8
So 1304686-93-8 is a valid CAS Registry Number.

1304686-93-8Upstream product

1304686-93-8Downstream Products

1304686-93-8Relevant academic research and scientific papers

A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Synthesis of catalyst libraries and evaluation of catalyst activity

Denmark, Scott E.,Gould, Nathan D.,Wolf, Larry M.

, p. 4260 - 4336 (2011)

Despite over three decades of research into asymmetric phase-transfer catalysis (APTC), a fundamental understanding of the factors that affect the rate and stereoselectivity of this important process are still obscure. This paper describes the initial stages of a long-term program aimed at elucidating the physical organic foundations of APTC employing a chemoinformatic analysis of the alkylation of a protected glycine imine with libraries of enantiomerically enriched quaternary ammonium ions. The synthesis of the quaternary ammonium ions follows a diversity-oriented approach wherein the tandem inter[4 + 2]/intra[3 + 2] cycloaddition of nitroalkenes serves as the key transformation. A two-part synthetic strategy comprised of (1) preparation of enantioenriched scaffolds and (2) development of parallel synthesis procedures is described. The strategy allows for the facile introduction of four variable groups in the vicinity of a stereogenic quaternary ammonium ion. The quaternary ammonium ions exhibited a wide range of activity and to a lesser degree enantioselectivity. Catalyst activity and selectivity are rationalized in a qualitative way on the basis of the effective positive potential of the ammonium ion.

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