91419-60-2 Usage
General Description
4-(1H-Tetrazol-5-yl)-piperidine hydrochloride is a chemical compound containing a piperidine ring and a tetrazole group. It is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs, particularly in the development of medications for cardiovascular and central nervous system disorders. The hydrochloride salt form of this compound makes it more stable and suitable for pharmacological applications. The presence of the tetrazole group in the structure also makes it a potential candidate for drug design due to its bioactive properties. Overall, 4-(1H-Tetrazol-5-yl)-piperidine hydrochloride is an important intermediate in the synthesis of pharmaceuticals with potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 91419-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,1 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91419-60:
(7*9)+(6*1)+(5*4)+(4*1)+(3*9)+(2*6)+(1*0)=132
132 % 10 = 2
So 91419-60-2 is a valid CAS Registry Number.
91419-60-2Relevant articles and documents
NOVEL IMIDAZOTRIAZINONE OR IMIDAZOPYRAZINONE DERIVATIVES, AND USE THEREOF
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Paragraph 332-334, (2016/04/26)
The present invention relates to novel a imidazotriazinone or imidazopyrazinone derivative, a tautomer thereof, a stereoisomer thereof and their mixture, or a pharmaceutically acceptable salt thereof; and a pharmaceutical composition for preventing or treating a tankyrase-related disease, which contains the same as an active ingredient.
Tetrazole analogues of GABA-mimetic agents
Schlewer,Wermuth,Chambon
, p. 181 - 186 (2007/10/02)
Six tetrazole analogues of GABA-mimetic compounds were synthesized. In vitro only two compounds, analogues of GABA and isoguvacine, showed a weak affinity for GABA-A and GABA-B receptors. In vivo compounds were inactive in a psychopharmacological screening in mice. The results were interpreted in terms of intercharge distance, electronic delocalisation and ability of membrane crossing.
