129865-52-7 Usage
General Description
2-PIPERIDIN-1-YL-THIAZOLE-5-CARBALDEHYDE is a chemical compound with the molecular formula C11H14N2OS. It is a heterocyclic compound that contains a piperidine ring and a thiazole ring with a carbonyl group attached to the fifth carbon atom of the thiazole ring. 2-PIPERIDIN-1-YL-THIAZOLE-5-CARBALDEHYDE is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various bioactive molecules and pharmaceutical intermediates. It has potential applications in the development of new drugs and agrochemicals due to its unique structural properties and reactivity. Additionally, it may also be used as a reagent in chemical reactions for the synthesis of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 129865-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,6 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 129865-52:
(8*1)+(7*2)+(6*9)+(5*8)+(4*6)+(3*5)+(2*5)+(1*2)=167
167 % 10 = 7
So 129865-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2OS/c12-7-8-6-10-9(13-8)11-4-2-1-3-5-11/h6-7H,1-5H2
129865-52-7Relevant articles and documents
Influence of thiazole regioisomerism on second-order nonlinear optical chromophores
Galán, Elena,Andreu, Raquel,Garín, Javier,Mosteo, Laura,Orduna, Jesús,Villacampa, Belén,Diosdado, Beatriz E.
experimental part, p. 6427 - 6437 (2012/09/05)
Two series of matched and mismatched donor-thiazole-acceptor chromophores have been synthesized to disclose the role that the orientation of the thiazole ring plays on their second-order nonlinear optical (NLO) properties. Whereas previous theoretical stu
An Easy General Synthesis of 2-(N,N-Dialkylamino)thiazol-5-yl Aldehydes and Ketones
Sawhney, Indu,Wilson, John R. H.
, p. 329 - 331 (2007/10/02)
Reaction between 2-chloro-5-thiazolyl-lithium and N,N-dialkylformamides or amides gave 2-N,N-dialkylaminothiazol-5-yl aldehydes or ketones on quenching with water.Quenching with acid gave 2-chlorothiazole-5-yl aldehydes or ketones, from which chloride was easily displaced by free amines.