104186-22-3 Usage
General Description
2,6-dimethyl-4-{[5-(pyridin-3-yl)-2H-tetrazol-2-yl]methyl}phenol, also known as M244, is a chemical compound with potential pharmacological properties. 2,6-dimethyl-4-{[5-(pyridin-3-yl)-2H-tetrazol-2-yl]methyl}phenol is a derivative of tetrazole and has been studied for its potential as a drug for treating conditions such as hypertension, cardiac arrhythmias, and heart failure. Its structure includes a phenol group, a tetrazole ring, and a pyridine ring, and it is believed to have antioxidant properties. M244 has shown promising results in preclinical studies, and its unique chemical structure makes it a potentially valuable candidate for future drug development. However, further research is needed to fully understand its pharmacological effects and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 104186-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104186-22:
(8*1)+(7*0)+(6*4)+(5*1)+(4*8)+(3*6)+(2*2)+(1*2)=93
93 % 10 = 3
So 104186-22-3 is a valid CAS Registry Number.
104186-22-3Relevant articles and documents
ALKYLATION OF 5-SUBSTITUTED 1-H-TETRAZOLES BY MANNICH BASES UNDER THE ACTION OF ULTRASOUND
Ishmetova, R. I.,Kitaeva, V. G.,Rusinov, L. G.
, p. 902 - 905 (2007/10/02)
Alkylation of 5-substituted 1-H-tetrazoles by Mannich bases - N-(3,5-dimethyl-4-hydroxybenzyl)piperidine and N-(2-hydroxy-3-methoxy-5-formylbenzyl)piperidine - under the action of ultrasound increases the yield of the desired products, reduces the reactio
ALKYLATION OF 5-SUBSTITUTED TETRAZOLES WITH MANNICH BASES
Kitaeva, V. G.,Ishmetova, R. I.,Latosh, N. I.,Voronina, N. M.
, p. 697 - 700 (2007/10/02)
Mixtures of N(1) and N(2) isomers are formed in the alkylation of 1H-5-R-tetrazoles with N-(2-hydroxy-3-methoxy-5-formylbenzyl)piperidine, whereas primarily one of two possible N(1) or N(2) isomers is formed in the case of alkylation with N-(3,5-dimethyl-4-hydroxybenzyl)piperidine, depending on substituent R.
