39254-63-2

Usage

Uses

Used in Pharmaceutical Industry:
Acetamidrazone HCL is used as an antitumor agent for its potential to target and treat cancer cells, offering a novel therapeutic approach in oncology.
Acetamidrazone HCL is used as an antiviral agent to combat viral infections, providing an alternative treatment strategy for viral diseases.
Acetamidrazone HCL is used as an anti-inflammatory and analgesic agent, helping to alleviate inflammation and pain associated with various conditions.
Used in Neurodegenerative Disorder Treatment:
Acetamidrazone HCL is used as a potential therapeutic agent for the treatment of neurodegenerative disorders, aiming to slow down or halt the progression of these diseases.
Used in Industrial Applications:
Acetamidrazone HCL is used as a chelating agent in the extraction and separation of metals, playing a crucial role in metal processing and purification.
Used in Organic Synthesis:
Acetamidrazone HCL is used as a reagent in organic synthesis, contributing to the development of new chemical compounds and materials.

InChI:InChI=1/C2H7N3.ClH/c1-2(3)5-4;/h4H2,1H3,(H2,3,5);1H

Upstream product

• 2208-07-3 ethyl acetimidate hydrochloride 
• 64-17-5 ethanol 
• 124-42-5 acetamidine hydrochloride 

Downstream Products

• 4076-36-2 5-methyl-1,2,3,4-tetrazole 
• 60576-67-2 N-acetimidoyl-N'-thiobenzoylhydrazine 
• 24108-33-6 3-methyl-1,2,4-triazine 
• 1450733-75-1 C₂₃H₂₉N₇O₃ 
• 38027-23-5 C₁₂H₁₆N₆ 
• 1130206-85-7 4,4'-(methylenedi-4,1-phenylene)bis(2,4-dihydro-5-methyl-3H-1,2,4-triazol-3-one) 
• 6232-84-4 4-allyl-5-methyl-1,2,4-triazole-3-thione 
• 60576-68-3 N'-(4-chloro-thiobenzoyl)-acetohydrazonic acid amide 
• 37496-83-6 C₁₀H₁₀N₄ 

Relevant academic research and scientific papers

PYRIDOXAL AMINOGUANIDINE DERIVATIVES AND THEIR SALTS AND PRODUCTION METHOD THEREOF

PROBLEM TO BE SOLVED: To provide compounds which are good in absorptivity on oral administration, serve as hypoglycemic agents with high safety and are useful as inhibitors for AGE formation reactions and their production method. SOLUTION: A method of producing pyridoxal/aminoguanidine derivatives and their salts having a structure with the amino group of pyridine derivatives of formula (V) substituted with another group comprises reacting pyridoxal with one of 1-amino-3-propyl guanidine hydroiodide, 4-methyl-S-methylisothiosemicarbazide hydroiodide, 3-methylisosemicarbazide hydrochloride and morpholine-4-carboxyimide hydrazide hydroiodide. COPYRIGHT: (C)2015,JPO&INPIT

Electronic properties of 3,3′-dimethyl-5,5'-bis(l,2,4-triazine): Towards design of supramolecular arrangements of N-heterocyclic Cui complexes

A new efficient and safe synthesis of 3,3′-dimethyl-5,5′-bis- (1,2,4-triazine) is presented. The electron-density distribution and electrostatic properties (charge, electrostatic potential) of this molecule were analyzed. These properties were derived from a high-resolution single-crystal X-ray diffraction experiment at 100 K and compared to the results obtained from ab initio DFT quantum-mechanical calculations. Comparisons of its electrostatic potential features and integrated atomic charges (quantum theory of atoms in molecules, QTAIM) havebeen made with those of related molecules such as bipyrimidine ligands. Two methods were used to derive integrated charges: one is based on the conventional analytical procedure and the second uses a steepest-ascent numerical algorithm. Excellent agreement was obtained between these two methods. Charges and electrostatic potential were used as predictive indices of metal chelation and discussed in the light of complexation abilities of the title compound and related molecules. The crystal structure of a Cu I complex of 3,3′-dimethyl-5,5′-bis(1,2,4-triazine) is reported here. In the solid state, this complex forms a three-dimensional multibranch network with open channels in which counterions and solvent molecules are located. This architecture involves both cis and trans isomers of the title compound.