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N-(2-chloro-4-nitrophenyl)thiomorpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

237432-05-2

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237432-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237432-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,4,3 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 237432-05:
(8*2)+(7*3)+(6*7)+(5*4)+(4*3)+(3*2)+(2*0)+(1*5)=122
122 % 10 = 2
So 237432-05-2 is a valid CAS Registry Number.

237432-05-2Relevant academic research and scientific papers

20-HYDROXYEICOSATETRAENOIC ACID PRODUCTION INHIBITORS

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Page 5, (2008/06/13)

A hydroxyformamidine compound represented by the following formula or a pharmaceutically acceptable salt thereof. [wherein R1 represents a substituted morpholino group, a substituted piperidino group, a piperazin-1-yl group, a substituted piperazin-1-yl group, a thiomorpholin-1-yl group, a perhydroazepin-1-yl group, a perhydroazocin-1-yl group, a tetrahydropyridin-1-yl group, a pyrrolin-1-yl group, etc.; X represents a nitrogen atom or a group represented by CR5; and R2 to R5 are the same or different and each represents a hydrogen atom, a C1-4 alkyl group, a C1-4 alkoxy group, a trifluoromethyl group or a halogen atom.] There is provided a drug which inhibi ts an enzyme producing 20-HETE participating in a contracting or dilating action for microvessels and an inducing action for cell proliferation in main organs such as kidney and cerebrovascular vessels.

N-[4-(1,1'-biphenylyl)methyl]-4-(4-thiomorpholinylmethyl) benzenamines, a new class of synthetic antituberculosis agents active against Mycobacterium avium

Mai, Antonello,Sbardella, Gianluca,Artico, Marino,Massa, Silvio,Lampis, Giorgio,Deidda, Delia,Pompeit, Raffaello

, p. 149 - 161 (2007/10/03)

Various N-derivatives of 4-(4-thiomorpholinyl)aniline and 4-(4- thiomorpholinylmethyl)aniline were synthesized and tested for in vitro antibacterial activities against Mycobacterium avium CIP 103317 and other mycobacteria including M. tuberculosis CIP 103471. Appropriate substituents were introduced at the nitrogen of aniline portion in order to exploit their potential antimycobacterial activities. Only derivatives with the biphenylylmethyl group bound to the 4-(4-thiomorpholinylmethyl)aniline moiety were found to possess appreciable antibacterial activities against atypical mycobacteria and M. tuberculosis. Several compounds (7c-g and 7j) were two and sixteen times more potent than azithromycin and isoniazid, respectively, in the in vitro assays against M. avium.

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