39205-64-6 Usage
Nitro-substituted pyrazole derivative
The compound is derived from a pyrazole ring (a five-membered heterocyclic ring with two nitrogen atoms) by substituting one of its positions with a nitro group (-NO2).
Building block in synthesis
1-Methyl-3-nitro-1H-pyrazole-4-carbonitrile is commonly used as a starting material or intermediate in the synthesis of various organic compounds, making it a valuable chemical in organic chemistry.
Potential applications in pharmaceutical and agrochemical industries
This chemical has possible uses in the development of new drugs and pesticides, making it an important precursor for creating products in these industries.
Unique structure and properties
The specific arrangement of atoms and the presence of different functional groups in the compound give it unique properties that make it valuable for various applications.
Creation of advanced materials and products
Due to its versatile chemical structure, 1-methyl-3-nitro-1H-pyrazole-4-carbonitrile can be used to develop materials and products with diverse uses across different industries.
Wide-ranging potential for innovative applications
The compound's versatility and unique properties make it a promising candidate for the development of new technologies and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 39205-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39205-64:
(7*3)+(6*9)+(5*2)+(4*0)+(3*5)+(2*6)+(1*4)=116
116 % 10 = 6
So 39205-64-6 is a valid CAS Registry Number.
39205-64-6Relevant academic research and scientific papers
Nitropyrazoles. 11. Isomeric 1-methyl-3(5)-nitropyrazole-4-carbonitriles in nucleophilic substitution reactions. Comparative reactivity of the nitro group in positions 3 and 5 of the pyrazole ring
Dalinger,Zaitsev,Shkineva,Shevelev
, p. 580 - 583 (2007/10/03)
With reactions of isomeric 1-methyl-3-nitro- and 1-methyl-5-nitropyrazole- 4-carbonitriles with anionic S-, O-, and N-nucleophiles (RSH, PhOH, and 3,5-dimethyl-4-nitropyrazole in the presence of K2CO3 or MeONa), it was shown that for
Anti-bacterial compositions containing certain 3-nitropyrazoles
-
, (2008/06/13)
Novel 1,4-disubstituted-3-nitropyrazoles having antimicrobial, parasiticidal, and herbicidal activity are prepared by a reaction sequence of which the individual steps are conventional. The new 3-nitropyrazoles are characterized by a 1-substituent and a usually carbonyl-containing 4-substituent. The novel 3(5)-nitro-4-pyrazole-carbonitrile is obtained as an intermediate in the preparation of the biologically-active compounds. Preferred compounds are 1-alkyl or -alkenyl-4-pyrazolecarboxamides and carbonitriles. The new compounds are particularly useful for the control of bacterial animal diseases.
