1214-75-1 Usage
Description
(N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB is a chemical compound characterized by the presence of a dimethylamino group and a 2,4-dinitrobenzene group. (N N-DIMETHYLAMINO)ETHENYL-2 4-DINITROB& is recognized for its explosive properties, which necessitates careful handling. It is widely utilized in the synthesis of various organic compounds and has garnered interest for its potential applications in the fields of materials science and pharmaceuticals. Further research and testing may reveal more uses and properties of this chemical.
Uses
Used in Organic Synthesis:
(N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB is employed as a key component in the synthesis of a variety of organic compounds. Its unique structure allows it to participate in numerous chemical reactions, making it a valuable asset in the creation of diverse molecules.
Used in Materials Science:
In the field of materials science, (N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB has been studied for its potential applications. Its properties may contribute to the development of new materials with specific characteristics, such as improved stability or enhanced reactivity.
Used in Pharmaceuticals:
The pharmaceutical industry has shown interest in (N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB due to its potential use in the development of new drugs. Its unique chemical structure may offer novel pathways for drug design and synthesis, potentially leading to the creation of more effective medications.
Used as a Reagent in Chemical Reactions:
(N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB may also serve as a reagent in various chemical reactions. Its reactive groups can participate in a range of processes, making it a useful tool for chemists in their quest to create new compounds and materials.
Used as a Precursor to Other Compounds:
Due to its unique structure, (N,N-DIMETHYLAMINO)ETHENYL-2,4-DINITROB can act as a precursor to other compounds. This means that it can be transformed into different molecules through chemical reactions, further expanding its utility in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1214-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1214-75:
(6*1)+(5*2)+(4*1)+(3*4)+(2*7)+(1*5)=51
51 % 10 = 1
So 1214-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O4/c1-11(2)6-5-8-3-4-9(12(14)15)7-10(8)13(16)17/h3-7H,1-2H3/b6-5+
1214-75-1Relevant articles and documents
Nitropyrazoles: XII. Transformations of the 4-methyl group in 1,4-dimethyl-3,5-dinitropyrazole and cyclization of the transformation products
Zaitsev,Dalinger,Starosotnikov,Kachala,Strelenko,Shkineva,Shevelev
, p. 1507 - 1515 (2007/10/03)
A preparative procedure for the synthesis of 1,4-dimethyl-3,5- dinitropyrazole by nitration of 1,4-dimethylpyrazole was developed. The reaction of 1,4-dimethyl-3,5-dinitropyrazole with dimethoxymethyl-(dimethyl)amine (N,N-dimethylformamide dimethyl acetal) gave (E)-N,N-dimethyl-2-(1-methyl-3,5- dinitropyrazol-4-yl)ethenylamine. Acid hydrolysis of the latter afforded (1-methyl-3,5-dinitropyrazol-4-yl)acetaldehyde, and the reaction with sodium nitrite in hydrochloric acid led to formation of 2-hydroxymino-2-(1-methyl-3,5- dinitropyrazol-4-yl)acetaldehyde. The corresponding O-methyloxime and phenylhydrazone reacted with K2CO3 to give 6-methyl-4-nitropyrazolo[4,3-d]isoxazole-3-carbaldehyde O-methyloxime and 1-methyl-3-nitro-4-(2-phenyl-2H-1,2,3-triazol-4-yl)pyrazol-5-ol, respectively. Treatment of (1-methyl-3,5-dinitropyrazol-4-yl)-acetaldehyde with benzenediazonium chloride gave (1-methyl-3,5-dinitropyrazol-4-yl)acetaldehyde phenylhydrazone which underwent intramolecular cyclization with replacement of the 5-nitro group by the action of K2CO3 in acetonitrile; in the reaction with K2CO3 in ethanol, the 5-nitro group was replaced by ethoxy.
