886501-12-8 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-4-piperidin-1-yl-benzaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals and research chemicals. Its unique structure allows it to be a key component in the development of antihistamines, antipsychotics, and other significant drugs. 2-CHLORO-4-PIPERIDIN-1-YL-BENZALDEHYDE's reactivity and functional groups enable the creation of a wide range of medicinal compounds with therapeutic potential.
Due to its toxic and irritating nature, 2-Chloro-4-piperidin-1-yl-benzaldehyde should be handled with caution and proper safety measures to ensure the well-being of those involved in its synthesis and use. Its role in the pharmaceutical industry is crucial, as it contributes to the advancement of new drug formulations and the improvement of existing treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 886501-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 886501-12:
(8*8)+(7*8)+(6*6)+(5*5)+(4*0)+(3*1)+(2*1)+(1*2)=188
188 % 10 = 8
So 886501-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClNO/c13-12-8-11(5-4-10(12)9-15)14-6-2-1-3-7-14/h4-5,8-9H,1-3,6-7H2
886501-12-8Relevant articles and documents
Piperidine compound and preparation method and medical application thereof
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Paragraph 0489-0508; 0509; 0514, (2021/04/07)
The invention discloses a piperidine compound shown as a formula (I) and a preparation method and medical application thereof, and particularly relates to a piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof and a preparation method and application of the piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof. The compound provided by the invention can inhibit the activity of USP7 enzyme, has very good selectivity and druggability, and can be used for preparing medicines for preventing or treating tumor diseases or virus infectious diseases.
Benzothiazines in organic synthesis. Synthesis of fluorescent 7-amino-2,1-benzothiazines
Yongpruksa, Nattawut,Pandey, Siddharth,Baker, Gary A.,Harmata, Michael
supporting information; experimental part, p. 7979 - 7982 (2012/01/04)
Fluorescent 7-amino-2,1-benzothiazines were prepared in high yields using the palladium-catalyzed reaction of 4-amino-2-chlorobenzaldehydes with a sulfoximine or the reaction of 7-fluoro-2,1-benzothiazines with amines. The Royal Society of Chemistry 2011.