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831191-89-0

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831191-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 831191-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,1,1,9 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 831191-89:
(8*8)+(7*3)+(6*1)+(5*1)+(4*9)+(3*1)+(2*8)+(1*9)=160
160 % 10 = 0
So 831191-89-0 is a valid CAS Registry Number.

831191-89-0Downstream Products

831191-89-0Relevant articles and documents

DERIVATIVES OF AMINOINDANES, THEIR PREPARATION AND THEIR APPLICATION IN THERAPEUTICS

-

, (2011/10/03)

The instant invention relates to derivatives of formula (I) and their application in therapeutics.

Synthesis of chiral building blocks for use in drug discovery

Marino, Sharon T.,Stachurska-Buczek, Danuta,Huggins, Daniel A.,Krywult, Beata M.,Sheehan, Craig S.,Nguyen, Thao,Choi, Neil,Parsons, Jack G.,Griffiths, Peter G.,James, Ian W.,Bray, Andrew M.,White, Jonathan M.,Boyce, Rustum S.

, p. 405 - 426 (2007/10/03)

In the past decade there has been a significant growth in the sales of pharmaceutical drugs worldwide, but more importantly there has been a dramatic growth in the sales of single enantiomer drugs. The pharmaceutical industry has a rising demand for chiral intermediates and research reagents because of the continuing imperative to improve drug efficacy. This in turn impacts on researchers involved in preclinical discovery work. Besides traditional chiral pool and resolution of racemates as sources of chiral building blocks, many new synthetic methods including a great variety of catalytic reactions have been developed which facilitate the production of complex chiral drug candidates for clinical trials. The most ambitious technique is to synthesise homochiral compounds from non-chiral starting materials using chiral metal catalysts and related chemistry. Examples of the synthesis of chiral building blocks from achiral materials utilizing asymmetric hydrogenation and asymmetric epoxidation are presented.

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