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116650-37-4

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116650-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116650-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,5 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116650-37:
(8*1)+(7*1)+(6*6)+(5*6)+(4*5)+(3*0)+(2*3)+(1*7)=114
114 % 10 = 4
So 116650-37-4 is a valid CAS Registry Number.

116650-37-4Downstream Products

116650-37-4Relevant articles and documents

Asymmetric chemoenzymatic synthesis of ramatroban using lipases and oxidoreductases

Busto, Eduardo,Gotor-Fernandez, Vicente,Gotor, Vicente

, p. 4842 - 4848 (2012/07/31)

A chemoenzymatic asymmetric route for the preparation of enantiopure (R)-ramatroban has been developed for the first time. The action of lipases and oxidoreductases has been independently studied, and both were found as excellent biocatalysts for the production of adequate chiral intermediates under very mild reaction conditions. CAL-B efficiently catalyzed the resolution of (±)-2,3,4,9-tetrahydro-1H-carbazol-3-ol that was acylated with high stereocontrol. On the other hand, ADH-A mediated bioreduction of 4,9-dihydro-1H-carbazol-3(2H)-one provided an alternative access to the same enantiopure alcohol previously obtained through lipase-catalyzed resolution, a useful synthetic building block in the synthesis of ramatroban. Inversion of the absolute configuration of (S)-2,3,4,9-tetrahydro-1H-carbazol-3-ol has been identified as a key point in the synthetic route, optimizing this process to avoid racemization of the azide intermediate, finally yielding (R)-ramatroban in enantiopure form by the formation of the corresponding amine and the convenient functionalization of both exocyclic and indole nitrogen atoms.

Synthesis and absolute configuration of the new thromboxane antagonist (3R)-3-(4-Fluorophenylsulfonamido)-1,2,3,4-tetrahydro-9- carbazolepropanoic acid and comparison with its enantiomer

Rosentreter,Boshagen,Seuter,Perzoborn,Fiedler

, p. 1519 - 1521 (2007/10/02)

The synthesis of (3R)-3-(4-Fluorophenylsulfonamido)-1,2,3,4-tetrahydro-9- carbazolepropanoic acid (Bay u 3405), a new, enantiomerically pure antagonist of thromboxane A2, is described. The determination of the absolute configuration of Bay u 3405 was performed by an X-ray analysis of compound 7 ([3((2S)-acetylamido)-3-phenylpropionamido]- 1,2,3,4-tetrahydro-carbazol). Bay u 3405 is in vitro 1 to 2 orders of magnitude more acitve than its (-)-enantiomer Bay u 3406.

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