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N-methyl-1-(3-methylbenzo[b]thiophen-2-yl)methanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335032-41-2

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335032-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335032-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,0,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 335032-41:
(8*3)+(7*3)+(6*5)+(5*0)+(4*3)+(3*2)+(2*4)+(1*1)=102
102 % 10 = 2
So 335032-41-2 is a valid CAS Registry Number.

335032-41-2Downstream Products

335032-41-2Relevant academic research and scientific papers

NOVEL COMPOUNDS AND THEIR USE

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Page/Page column 104-105, (2021/06/26)

The present invention provides compounds of the general formula (I) or a pharmaceutically acceptable prodrugs, salts and/or solvates thereof, wherein LHS is selected from the group consisting of LHSa and LHSb And wherein, the asterisk (*) marks the point of attachment; These compounds exhibit antibacterial activity against Gram-negative and Gram-positive bacteria, especially S. aureus, E. coli, K. pneumoniae and A. baumannii. Pharmaceutical compositions containing these compounds, therapeutic uses thereof and methods for manufacturing the same are also provided.

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF FATTY ACID BIOSYSNTHESIS FOR BACTERIAL INFECTIONS

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Paragraph 0036; 0037, (2014/09/16)

The present invention relates to novel heterocyclic compounds which specifically inhibit bacterial FabI and can be used for the treatment of Staphylococcal infections.

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF FATTY ACID BIOSYNTHESIS FOR BACTERIAL INFECTIONS

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Page/Page column 11, (2013/04/10)

The present invention relates to novel heterocyclic compounds which specifically inhibit bacterial Fab I and can be used for the treatment of Staphylococcal infections.

FAB I INHIBITORS

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, (2008/06/13)

Compounds of the formula (I) are disclosed which are Fab I inhibitors and are useful in the treatment of bacterial infections.

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