36286-75-6

Usage

Uses

Used in Agricultural Industry:
4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE is used as a pesticide and herbicide for the control of weeds in agricultural settings. It helps to protect crops from unwanted plant growth, thereby ensuring higher yields and better crop quality.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE is used as an intermediate in the production of various pharmaceuticals. Its chemical properties make it a valuable component in the synthesis of drugs that address a range of health conditions.
Used in Organic Compounds Synthesis:
4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE is also utilized in the synthesis of other organic compounds. Its unique structure allows it to be a key building block in the creation of various chemical products used in different industries.
Environmental Considerations:
Given its potential for causing harm to aquatic life and the environment, 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE must be used and disposed of properly. It is crucial to follow safety guidelines and regulations to minimize its impact on the environment and human health.

InChI:InChI=1/C7H8ClN3/c8-6-3-1-5(2-4-6)7(9)11-10/h1-4H,10H2,(H2,9,11)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 64-17-5 ethanol 

Downstream Products

• 1003046-47-6 3-(p-chlorophenyl)phenanthro[9,10-e][1,2,4]triazine 
• 62230-37-9 3-(4-chlorophenyl)-5-phenyl-1,2,4-triazine 
• 89730-55-2 6-Amino-3-(4-chlorphenyl)-1,2,4-triazin-5(2H)-on 
• 126542-16-3 3-(4-Chloro-phenyl)-5-oxo-2,5-dihydro-[1,2,4]triazine-6-carboxylic acid methyl ester 
• 81945-81-5 7-(4-Chloro-phenyl)-2,3a,5-triphenyl-3,3a-dihydro-pyrazolo[1,5-c]pyrimidine 
• 109948-30-3 3-(4-Chloro-phenyl)-5-[(2-oxo-1,2-diphenyl-ethyl)-phenyl-amino]-1H-[1,2,4]triazin-6-one 
• 126542-15-2 3-(4-Chloro-phenyl)-6-phenyl-2H-[1,2,4]triazin-5-one 
• 36286-77-8 ethyl 3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1,2,4-triazine-6-carboxylate 
• 89730-63-2 6-Amino-3-(4-chlorphenyl)-1,2,4-triazin-5(2H)-thion 
• 87522-18-7 2-p-chlorophenyl-4-oxido-6,8-diphenylpyrido<2,1-f><1,2,4>triazin-9-ium 
• 126542-77-6 5-But-3-ynyloxy-3-(4-chloro-phenyl)-6-phenyl-[1,2,4]triazine 
• 126542-26-5 5-Chloro-3-(4-chloro-phenyl)-[1,2,4]triazine-6-carboxylic acid methyl ester 
• 126542-25-4 5-Chloro-3-(4-chloro-phenyl)-6-phenyl-[1,2,4]triazine 
• 126542-35-6 ethyl 5-chloro-3-(4-chlorophenyl)-1,2,4-triazine-6-carboxylate 

Relevant academic research and scientific papers

Novel 6-azapteridines from bifunctional 1,2,4-triazines

The convergent synthesis of ethyl 5-chloro- and 5-amino-3-aryl-1,2,4-triazinecarboxylates 9a-9d and 10a-10d as well as of 5-amino-3-aryl-1,2,4-triazine-6-carboxamides 11a-11d is described. Compounds 9, 10 and 11 are powerful key compounds for cyclization reactions to the novel pyrimido[4,5-e][1,2,4]triazines 13d, 14c, 14d, 15c and 17a, 17d.

Amidrazones and derivatives thereof

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging) which contain novel amidrazones and derivatives thereof. Accordingly, a composition is disclosed which comprises an agent capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.