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benzyl (trans)-7-oxooctahydro-2H-cyclopenta[c]pyridine-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140211-06-9

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140211-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140211-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,2,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140211-06:
(8*1)+(7*4)+(6*0)+(5*2)+(4*1)+(3*1)+(2*0)+(1*6)=59
59 % 10 = 9
So 140211-06-9 is a valid CAS Registry Number.

140211-06-9Relevant academic research and scientific papers

Azabicyclic compounds are central nervous system active agents

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Page 58, (2010/02/05)

Compounds of formula (I) are novel CNS active agents that are useful for treating pain and for treating other disorders associated with the cholinergic system.

Synthesis and antibacterial activity of new 7-(aminoazabicycloalkanyl)quinolonecarboxylic acids

Ogata, M,Matsumoto, H,Shimizu, S,Kida, S,Nakai, H,et al.

, p. 889 - 906 (2007/10/02)

A series of novel 7--6-fluoro-1-substituted quinolinecarboxylic acids (18-53) have been prepared and their antibacterial activities evaluated.These compounds are characterized structurally by a new amino-substituted azabicyclooctane, -nonane and -decane ring systems at the 7-position of quinolonecarboxylic acids.To compare the biological activities of enantiomers, (+)-7-octan-3-yl>-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolonecarboxylicacid hydrochloride (43, 44) were synthesized and evaluated for antibacterial activity.Compound 43 was more potent than 44 against both Gram-positive and Gram-negative organisms.The structure-activity relationships of these quinolonecarboxylic acids are also discussed. antibacterial activity / amino-substituted azabicycloalkane ring / substituted quinolonecarboxylic acids / structure-activity relationships

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