145769-58-0 Usage
Chemical Classification
Nitroamine
Explanation
Different sources of media describe the Explanation of 145769-58-0 differently. You can refer to the following data:
1. Nitroamines are a class of compounds that contain both an amino group (-NH2) and a nitro group (-NO2). They are known for their potential reactivity and toxicity.
2. The 1,2,3-triazole ring is a five-membered heterocyclic ring containing three nitrogen atoms and two carbon atoms. It is a common structural motif in various chemical compounds.
3. The amino group (-NH2) is attached to the fourth position of the 1,2,3-triazole ring, which is one of the carbon atoms in the ring.
4. The nitro group (-NO2) is attached to the fifth position of the 1,2,3-triazole ring, which is the other carbon atom in the ring.
5. 1H-1,2,3-Triazol-4-amine,5-nitro-(9CI) has been studied for its potential use in the development of pharmaceuticals and agrochemicals due to its unique chemical structure and properties.
6. This compound can serve as a building block in organic synthesis, which is the process of constructing complex organic molecules from simpler ones.
7. Due to its potential toxicity and reactivity, it is important to handle 1H-1,2,3-Triazol-4-amine,5-nitro-(9CI) with care and follow proper safety protocols.
8. More research is required to fully understand the properties, potential uses, and safety concerns associated with 1H-1,2,3-Triazol-4-amine,5-nitro-(9CI) in various industries.
Structural Feature
1,2,3-Triazole ring
Amino Group Position
4
Nitro Group Position
5
Potential Applications
Pharmaceuticals and Agrochemicals
Role in Organic Synthesis
Building Block
Safety Precautions
Handle with caution
Research Status
Further research needed
Check Digit Verification of cas no
The CAS Registry Mumber 145769-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,6 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145769-58:
(8*1)+(7*4)+(6*5)+(5*7)+(4*6)+(3*9)+(2*5)+(1*8)=170
170 % 10 = 0
So 145769-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H3N5O2/c3-1-2(7(8)9)5-6-4-1/h(H3,3,4,5,6)
145769-58-0Relevant articles and documents
GEM-DINITRO COMPOUNDS IN ORGANIC SYNTHESIS. 3. SYNTHESES OF 4-NITRO-1,2,3-TRIAZOLES FROM GEM-DINITRO COMPOUNDS
Baryshnikov, A. T.,Erashko, V. I.,Zubanova, N. I.,Ugrak, B. I.,Shevelev, S. A.,et al.
, p. 751 - 757 (2007/10/02)
Several chemoselective syntheses have been developed for 4-nitro-1,2,3-triazoles from sodium azide and gem-dinitroethylenes prepared from readily available transformation products of dinitroacetic acid ester: N-(β,β-dinitroethyl)-N,N-dialkylamines, 2,2-dinitroethanol acetate, a mixture of dinitroacetic acid ester with aliphatic aldehydes, or 1,1,1-trinitroalkanes.Hitherto-unknown 4-nitro-5-amino- and 4,5-dinitro-1,2,3-triazoles have been synthesized via successive transformations of the CH3 groups in 5-nitro-4-methyltriazole.Nitration of 4-nitro-1,2,3-triazole with nitronium fluoroborate or acetyl nitrate gave an unknown 2,4-dinitro-1,2,3-triazole.Keywords: gem-dinitro compounds, 4-nitro-1,2,3-triazoles, gem-dinitroethylenes, dinitroacetic acid ester, N-(β,β-dinitroethyl)-N,N-dialkylamines, 2,2-dinitroethanol acetate, 1,1,1-trinitroalkanes, nitration, cyclization, 2,4-dinitro-1,2,3-triazole.
