165670-57-5 Usage
General Description
2-(1-Methyl-1-phenylethyl)-5-phenyl-2H-tetrazole is a chemical compound with the molecular formula C17H18N4. It is a tetrazole derivative, which is a class of compounds known for their diverse biological activities. This particular compound has been studied for its potential antihypertensive and vasodilator effects, as well as its ability to inhibit platelet aggregation. It has also been investigated for its potential use as a functional food ingredient due to its antioxidant properties. Additionally, tetrazole derivatives like this compound have been studied for their potential applications in the treatment of various diseases, including cancer, diabetes, and inflammation. Further research is needed to fully understand and harness the potential pharmacological properties of 2-(1-Methyl-1-phenylethyl)-5-phenyl-2H-tetrazole.
Check Digit Verification of cas no
The CAS Registry Mumber 165670-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,6,7 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 165670-57:
(8*1)+(7*6)+(6*5)+(5*6)+(4*7)+(3*0)+(2*5)+(1*7)=155
155 % 10 = 5
So 165670-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H16N4/c1-16(2,14-11-7-4-8-12-14)20-18-15(17-19-20)13-9-5-3-6-10-13/h3-12H,1-2H3
165670-57-5Relevant articles and documents
Electrochemical Decarboxylative N-Alkylation of Heterocycles
Baran, Phil. S.,He, Chi,Shang, Ming,Sheng, Tao,Vantourout, Julien. C.,Zhang, Hai-Jun
supporting information, p. 7594 - 7598 (2020/10/09)
An operationally simple method to employ nonactivated carboxylic acids as alkylating agents in the N-alkylation of heterocycles is reported through an electrochemically driven anodic decarboxylative process. A wide substrate scope across a range of heterocycles is demonstrated along with a series of applications that significantly reduce the step count required to access such medicinally relevant structures.
Processes for preparing 1-butyl-2-[2'-(2H-tetrazol-5-yl) biphenyl-4-ylmethyl]-1H-indole-3-carboxylic acid
-
, (2008/06/13)
The present invention relates to processes for preparing 1-butyl-2-[2''-(2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-1H-indole-3-carboxylic acid and to intermediates useful in such processes. The present invention also relates to a process for deprotecting compounds containing a protected 2H-tetrazolyl group, which process comprises reacting a the protected compound with a Lewis acid in the presence of a thiol.
