1256268-95-7 Usage
Uses
Used in Pharmaceutical Industry:
3-(Methylamino)pyridazine-4-carbonitrile is used as a key intermediate for the synthesis of biologically active molecules, contributing to the development of new drugs. Its pharmacological properties have been studied, indicating its potential in the creation of therapeutic agents for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(Methylamino)pyridazine-4-carbonitrile is utilized as a precursor in the synthesis of pesticidal compounds. Its pesticidal properties have been investigated, showcasing its potential in the formulation of crop protection products that can enhance agricultural yields and protect crops from pests.
Used in Medicinal Chemistry Research:
3-(Methylamino)pyridazine-4-carbonitrile is employed as a valuable research molecule in medicinal chemistry. Its unique structural features make it an important intermediate for the synthesis of a diverse range of chemical compounds, facilitating advancements in drug discovery and development.
Used in Agricultural Chemistry Research:
Similarly, in agricultural chemistry, 3-(Methylamino)pyridazine-4-carbonitrile serves as a crucial molecule for research. Its role in the synthesis of agrochemicals aids in the exploration of new crop protection strategies and the improvement of existing products.
Check Digit Verification of cas no
The CAS Registry Mumber 1256268-95-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,2,6 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1256268-95:
(9*1)+(8*2)+(7*5)+(6*6)+(5*2)+(4*6)+(3*8)+(2*9)+(1*5)=177
177 % 10 = 7
So 1256268-95-7 is a valid CAS Registry Number.
1256268-95-7Relevant academic research and scientific papers
Synthesis of ortho-functionalized 4-aminomethylpyridazines as substrate-like semicarbazide-sensitive amine oxidase inhibitors
Haider, Norbert,Hochholdinger, Iris,Matyus, Peter,Wobus, Andrea
experimental part, p. 964 - 970 (2010/09/06)
A series of 4-aminomethylpyridazines and -pyridazin-3(2H)-ones ( diaza-benzylamines ), bearing alkylamino side chains in ortho position relative to the CH2NH2 unit, was synthesized by catalytic hydrogenation of the corresponding nitriles in strongly acidic medium. N-Benzyl protecting groups either at the pyridazinone ring nitrogen or at an exocyclic nitrogen were selectively removed hydrogenolytically or by treatment with a Lewis acid. The new compounds were tested in vitro for semicarbazide-sensitive amine oxidase (SSAO) inhibitory activity and 4-(aminomethyl)-N,N-diethylpyridazine-3,5-diamine (22) was found to be the most active representative.
