66012-75-7 Usage
Tetrazole derivative
PTZT contains two tetrazole rings, which are five-membered heterocyclic rings with four nitrogen atoms and one carbon atom.
Phenyl group
PTZT includes a phenyl group, which is a carbon ring with six carbon atoms and five hydrogen atoms, attached to one of the tetrazole rings.
High-energy compound
PTZT has a high energy content, making it suitable for use in propellants and explosives.
Thermal stability
PTZT exhibits good thermal stability, meaning it can withstand high temperatures without decomposing or losing its properties.
High heat of formation
PTZT has a high heat of formation, indicating that it requires a significant amount of energy to produce, which is beneficial for its use in energetic materials.
Potential applications
PTZT has potential applications in the field of propellants and explosives due to its high energy content and stability.
Unique molecular structure
PTZT's molecular structure, containing a phenyl group and two tetrazole rings, makes it attractive for further research and development in the field of energetic materials and pyrotechnics.
Check Digit Verification of cas no
The CAS Registry Mumber 66012-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,1 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66012-75:
(7*6)+(6*6)+(5*0)+(4*1)+(3*2)+(2*7)+(1*5)=107
107 % 10 = 7
So 66012-75-7 is a valid CAS Registry Number.
66012-75-7Relevant academic research and scientific papers
Tetrazoles: XL. Structure and basicity of 1,1′-disubstituted 5,5′-bitetrazoles
Ostrovskii,Kochkina,Shcherbinin,Koldobskii
, p. 1824 - 1830 (2007/10/03)
1,1′-Diaryl-5,5′-bitetrazoles, unlike 1,1′-dimethyl derivative, are Hammett bases which are much weaker than their monocyclic analogs. Bitetrazoles undergo monoprotonation in the H0 range from -5 to -9, and their pKBH+ values correla
Preparation of 1,5-disubstituted tetrazoles under phase-transfer conditions
Artamonova,Zhivich,Dubinskii,Koldobskii
, p. 1428 - 1430 (2007/10/03)
Imidoyl chlorides, obtained by common methods from a wide range of aromatic mono- and diamides, are smoothly converted to the corresponding tetrazoles in high yields by treatment with NaN3 under phase-transfer conditions.
