112633-15-5 Usage
Chemical class
Tetrazocines Tetrazocines are organic compounds containing a tetrazocine ring system.
High-energy material (HEM)
Yes It is classified as a high-energy material due to its high energy content.
Application
Energetic materials Used as an intermediate in the synthesis of energetic materials like explosives and propellants.
Stability
Highly stable The compound is known for its stability, making it suitable for various applications.
Energy content
High It has a high energy content, which contributes to its use in energetic materials.
Military and industrial applications
Suitable Due to its stability and high energy content, it is suitable for use in military and industrial applications.
Rocket propulsion
Potential candidate It has been studied for its potential use in rocket propulsion due to its explosive properties.
Pyrotechnics
Potential candidate It is also a potential candidate for use in pyrotechnics.
Pharmaceutical potential
Studied The compound has been studied for its potential use in pharmaceuticals and as a scaffold for drug design.
Check Digit Verification of cas no
The CAS Registry Mumber 112633-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,3 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112633-15:
(8*1)+(7*1)+(6*2)+(5*6)+(4*3)+(3*3)+(2*1)+(1*5)=85
85 % 10 = 5
So 112633-15-5 is a valid CAS Registry Number.
112633-15-5Relevant academic research and scientific papers
Revisitation of Formaldehyde-Aniline Condensation. III. The Cyclic Tetramer of N-Methyleneaniline: An X-Ray Diffraction Structure Determination
Randaccio, Lucio,Zangrando, Ennio,Gei, Maria H.,Giumanini, Angelo G.
, p. 187 - 194 (2007/10/02)
The cyclic tetramer of N-methyleneaniline, one of the products from the condensation between formaldehyde and aniline under neutral condition, has been characterized as 1,3,5,7-tetraphenyltetrazocine (3) and its crystal structure elucidated by X-ray diffraction.
Revisitation of Formaldehyde Aniline Condensation. VII. 1,3,5-Triarylhexahydro-sym-triazines and 1,3,5,7-Tetraaryl-1,3,5,7-tetrazocines from Aromatic Amines and Paraformaldehyde
Giumanini, Angelo G.,Verardo, Giancarlo,Zangrando, Ennio,Lassiani, Lucia
, p. 1087 - 1103 (2007/10/02)
A product study of the reaction between a number of aromatic amines substituted with widely different groups and paraformaldehyde in inert solvents was performed and found to yield 1,3,5-triaryl-1,3,5-hexahydrotriazines, 1,3,5,7-tetraaryl-1,3,5,7-tetrazocines and formaminals.It was not possible to correlate the product outcomes with the actual structure of the amine substrate.The X-ray diffraction structural determination of 1,3,5-tri-(t-butylphenyl)- (1b) and 1,3,5-tri-(m-fluorophenyl)-1,3,5-hexahydrotriazine (1c) showed the diaxial arrangement of the N-substituents.
