5817-87-8 Usage
Type of compound
Derivative of tetrazole
Industrial applications
a. Precursor in the production of pharmaceuticals
b. Precursor in the production of explosives
Structure
a. Cyclic
b. Heterocyclic compound
Metal ion interaction
Forms stable complexes with metal ions
Utility in coordination polymers
Useful in the design and synthesis of coordination polymers and materials
Stabilizer
Used as a stabilizer in propellants, fuels, and as a corrosion inhibitor in oil and gas production
Potential applications
Wide range of potential applications due to unique structure and properties
Check Digit Verification of cas no
The CAS Registry Mumber 5817-87-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5817-87:
(6*5)+(5*8)+(4*1)+(3*7)+(2*8)+(1*7)=118
118 % 10 = 8
So 5817-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4/c1-2-4-5-6-7-8(4)3-1/h1-3H2
5817-87-8Relevant academic research and scientific papers
Proximity-assisted cycloaddition reactions - Facile Lewis acid-mediated synthesis of diversely functionalized bicyclic tetrazoles
Hanessian, Stephen,Simard, Daniel,Deschenes-Simard, Benoit,Chenel, Caroline,Haak, Edgar
body text, p. 1381 - 1384 (2009/04/18)
(Chemical Equation Presented) Aliphatic azidonitriles separated by three or four carbon atoms undergo facile Lewis acid-induced cycloadditions to give bicyclic tetrazoles, even at 0 °C. Extension to 3-azido-2-aryl-1,3- dioxolanes and the corresponding 1,3-dioxanes in the presence of TMSCN and BF3·OEt2 leads to a series of diversely functionalized novel oxabicyclic tetrazoles. The reactions represent new aspects of proximity-assisted dipolar cycloadditions that afford thermodynamically controlled enantiopure products proceeding through discrete oxocarbenium ion intermediates.
