199014-14-7 Usage
Uses
As of now, the specific applications of 1-[(4-Methoxyphenyl)methyl]-1H-1,2,4-triazole-5-methanol are not well-documented. However, given its structural features, it is possible that the compound may find use in the following areas:
Used in Pharmaceutical Industry:
1-[(4-Methoxyphenyl)methyl]-1H-1,2,4-triazole-5-methanol could be used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its heterocyclic nature and functional groups may allow it to interact with biological targets, potentially leading to the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 1-[(4-Methoxyphenyl)methyl]-1H-1,2,4-triazole-5-methanol may serve as a model compound for studying the properties and reactivity of heterocyclic compounds. Its unique structure could provide insights into the behavior of similar compounds and contribute to the advancement of synthetic chemistry.
Used in Material Science:
1-[(4-Methoxyphenyl)methyl]-1H-1,2,4-triazole-5-methanol's polarity and functional groups may also make it a candidate for use in the development of new materials. It could potentially be incorporated into polymers, coatings, or other materials to impart specific properties, such as improved adhesion, stability, or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 199014-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,0,1 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 199014-14:
(8*1)+(7*9)+(6*9)+(5*0)+(4*1)+(3*4)+(2*1)+(1*4)=147
147 % 10 = 7
So 199014-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3O2/c1-16-10-4-2-9(3-5-10)6-14-11(7-15)12-8-13-14/h2-5,8,15H,6-7H2,1H3
199014-14-7Relevant academic research and scientific papers
Process and intermediates for preparing 4'-trifluoromethylbiphenyl-2-carboxylic acid [2-(2H-[1,2,4]triazol-3-ylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-yl]-a mide
-
, (2008/06/13)
A process for preparing the compound of formula (1) is disclosed. STR1 The starting materials are an N-triazolylmethyl-6-aminoisoquinoline and a 4-biphenyl-2-carboxylic acid derivative.
An efficient synthesis of 6-substituted 2-(2H-[1,2,4]triazol-3- ylmethyl)-1,2,3,4-tetrahydro-isoquinolines
Urban, Frank J.,Breitenbach, Ralph
, p. 645 - 653 (2007/10/03)
A synthesis of 6-nitro and 6-amino 2-(2H-[1,2,4]triazol-3- ylmethyl)1,2,3,4-tetrahydro-isoquinolines using a bis-alkylation process is described. 5-(Aminomethyl)-1-(p-methoxybenzyl)-triazole was prepared by a regioselective route from 1,2,4-triazole.
