114064-76-5 Usage
Chemical class
Hydrazone derivative of a tetrazole compound
Tetrazole group
A five-membered heterocyclic ring with four nitrogen atoms and one carbon atom
Hydrazine derivative
Contains a covalently bonded hydrazine (N2H4) group
Nitro-substituted
A nitro group (-NO2) is attached to the phenyl ring
Phenyl group
A six-membered aromatic ring with alternating single and double carbon-carbon bonds, attached to the nitrogen atom
Building block
Used in organic synthesis and pharmaceutical research for creating heterocyclic compounds and potential drug candidates
Unique structure
The combination of tetrazole, hydrazine derivative, and nitro-substituted phenyl group gives 1H-Tetrazol-5-amine,
1-[2,2-dimethyl-1-[(4-nitrophenyl)hydrazono]propyl]-N-phenyl- its distinctive properties
Reactivity
The compound exhibits specific reactivity due to its structure, making it useful as an intermediate in chemical and pharmaceutical material development
Check Digit Verification of cas no
The CAS Registry Mumber 114064-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,6 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114064-76:
(8*1)+(7*1)+(6*4)+(5*0)+(4*6)+(3*4)+(2*7)+(1*6)=95
95 % 10 = 5
So 114064-76-5 is a valid CAS Registry Number.
114064-76-5Relevant academic research and scientific papers
SYNTHESIS AND THERMOLYSIS OF SOME N-HYDROXIMOYL- AND N-HYDRAZONOYLAZOLES
Plenkiewicz, Jan,Zdrojewski, Tadeusz
, p. 675 - 710 (2007/10/02)
The reactions of nitrile oxides or nitrile imines with pyrazole, imidazole, 1,2,3- and 1,2,4-triazole or tetrazole derivatives yield the appropriate N-hydroximoyl- or N-hydrazonoylazoles.Thermolysis of 1-hydroximoyltetrazoles, depending on the nature of the substituents in the tetrazole ring, yields 1,2,4-oxadiazoles or 5-amino-1,2,4-oxadiazoles upon hydrazoic acid or nitrogen evolution.Under similar conditions, 1-hydrazonoyltetrazoles give 1,2,4-triazoles or 5-amino-1,2,4-triazoles while 2-hydrazonoyltetrazoles decompose to the dihydro-1,2,4,5-tetrazine derivatives.
