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2-azepanylmethanol(SALTDATA: FREE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19168-71-9

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19168-71-9 Usage

Classification

Alcohol

Structure

Contains a seven-membered azepane ring

Uses

Building block in organic synthesis, pharmaceutical research, production of pharmaceutical drugs, agrochemicals, chiral auxiliary in asymmetric synthesis

Potential applications

Production of pharmaceutical drugs, agrochemicals, and other fine chemicals
Versatile and valuable compound in organic chemistry field

Check Digit Verification of cas no

The CAS Registry Mumber 19168-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19168-71:
(7*1)+(6*9)+(5*1)+(4*6)+(3*8)+(2*7)+(1*1)=129
129 % 10 = 9
So 19168-71-9 is a valid CAS Registry Number.

19168-71-9Relevant academic research and scientific papers

2-AMINOPYRIDINES AS INHIBITORS OF CYCLOOXYGENASE-2

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Page/Page column 28, (2010/02/11)

The invention encompasses the novel compound of Formula (I) as well as a method of treating cyclooxygenase-2 mediated diseases comprising administration to a patient in need of such treatment of a non-toxic therapeutically effective amount of a compound of Formula (I). The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula (I).

Heterocyclic metalloprotease inhibitors

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, (2008/06/13)

The invention provides compounds of formula as described in the claims, or an optical isomer, diastereomer or enantiomer thereof, or a pharmaceutically-acceptable salt, or biohydrolyzable amide, ester, or imide thereof are useful as inhibitors of metallop

Design, synthesis, and biological evaluation of potent thiazine- and thiazepine-based matrix metalloproteinase inhibitors

Almstead, Neil G.,Bradley, Rimma S.,Pikul, Stanislaw,De, Biswanath,Natchus, Michael G.,Taiwo, Yetunde O.,Gu, Fei,Williams, Lisa E.,Hynd, Barbara A.,Janusz, Michael J.,Dunaway, C. Michelle,Mieling, Glen E.

, p. 4547 - 4562 (2007/10/03)

The synthesis and enzyme inhibition data for a series of thiazine- and thiazepine-based matrix metalloproteinase (MMP) inhibitors are described. The thiazine- and thiazepine-based inhibitors were discovered by optimization of hetererocyclic sulfonamide-ba

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