159583-34-3 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Pyridazineethanamine, tetrahydro-2-methyl-(9CI) is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Research and Development:
In the research and development sector, 1(2H)-Pyridazineethanamine, tetrahydro-2-methyl-(9CI) serves as a valuable compound for studying the properties and behavior of heterocyclic compounds. Its structure can be further modified to explore new chemical reactions and synthesize novel compounds with potential applications in various fields.
Used in Chemical Synthesis:
1(2H)-Pyridazineethanamine, tetrahydro-2-methyl-(9CI) is used as an intermediate in the synthesis of various chemical products. Its unique structure and functional groups make it a versatile building block for creating a wide range of compounds with different properties and applications.
Used in Material Science:
1(2H)-Pyridazineethanamine,tetrahydro-2-methyl-(9CI) may also find applications in material science, where its unique structure and properties can be utilized to develop new materials with specific characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 159583-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 159583-34:
(8*1)+(7*5)+(6*9)+(5*5)+(4*8)+(3*3)+(2*3)+(1*4)=173
173 % 10 = 3
So 159583-34-3 is a valid CAS Registry Number.
159583-34-3Relevant academic research and scientific papers
Synthesis of p-aminobenzamides of aminopiperidazines as potential antiarrhythmic agents
Kornet,Abdul-Nabi Ali,Steinberg
, p. 967 - 971 (2007/10/02)
1,2-Dimethyl-4-aminopiperidazine (4), 1-(2-aminoethyl)-2-methylpiperidazine (11), 2-(2-aminoethyl)-3-methyl-2,3-diazabicyclo[2.2.1]heptane (16), and 1,2-dimethyl-3-aminomethylpiperidazine (21) have been synthesized. Amines 4, 11, and 16 were converted to the corresponding p-nitrobenzamides 7, 12, and 17. Catalytic reduction of the latter nitro derivatives gave the corresponding p-aminobenzamides 8, 13, and 18. For comparative studies, the acyclic analog, 4-amino-N-[2-(1,1,2-trimethylhydrazino)ethyl]benzamide (25) was also synthesized. Compounds 8, 13 and 25 which are analogs of procainamide were evaluated in the isolated cardiac Purkinje fiber preparation by measuring their effects on the action potential upstroke velocity.
