5340-04-5 Usage
Uses
Used in Organic Synthesis:
1-PROPYL-1H-TETRAZOL-5-YLAMINE is used as a building block for the preparation of various biologically active compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
1-PROPYL-1H-TETRAZOL-5-YLAMINE is used as a reagent in chemical reactions, particularly in the development of new pharmaceuticals. Its ability to form stable complexes with other molecules makes it a promising candidate for drug discovery and design.
Used in the Synthesis of Heterocyclic Compounds:
As a propyl derivative of tetrazole, 1-PROPYL-1H-TETRAZOL-5-YLAMINE is used as a precursor for the synthesis of heterocyclic compounds. These compounds have a wide range of applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 5340-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5340-04:
(6*5)+(5*3)+(4*4)+(3*0)+(2*0)+(1*4)=65
65 % 10 = 5
So 5340-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N5/c1-2-3-9-4(5)6-7-8-9/h2-3H2,1H3,(H2,5,6,8)
5340-04-5Relevant academic research and scientific papers
9H-Xanthene-9-carboxylic acid [1,2,4]oxadiazol-3-yl- and (2H-tetrazol-5-yl)-amides as potent, orally available mGlu1 receptor enhancers
Vieira, Eric,Huwyler, Joerg,Jolidon, Synese,Knoflach, Frederic,Mutel, Vincent,Wichmann, Juergen
, p. 4628 - 4631 (2007/10/03)
Small molecule mGluR1 enhancers based on the lead compound (9H-xanthene-9-carbonyl)-carbamic acid butyl ester derived from random-screening hit diphenylacetyl-carbamic acid ethyl ester were designed and synthesized as useful pharmacological tools for the study of the physiological roles mediated by mGlu1 receptors. The synthesis and the structure-activity relationship of this new class of positive allosteric modulators of mGlu1 receptors will be discussed in detail.
