3775-60-8

Usage

Uses

Used in Pharmaceutical Industry:
NSC45356 is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, NSC45356 serves as a vital component in the creation of pesticides and other agricultural chemicals, leveraging its chemical properties to enhance crop protection and yield.
Used in Electronics Industry:
NSC45356 is utilized as a material in the electronics industry for its role in the development of electronic components and materials, capitalizing on its unique properties to improve device performance and reliability.
Used in Polymer Production:
NSC45356 is used as a monomer or a building block in the production of polymers, where its structural characteristics are essential for tailoring the properties of the resulting polymers for specific applications.
Used in Chemical Synthesis:
As a versatile chemical compound, NSC45356 is employed as a starting material in various chemical synthesis processes, enabling the creation of a wide range of industrial chemicals and specialty products.

InChI:InChI=1/C2H3N3O/c3-2-5-4-1-6-2/h1H,(H2,3,5)

Upstream product

• 506-68-3 bromocyane 
• 624-84-0 formic acid hydrazide 
• 74949-72-7 2-Amino-5-acetyl-1,3,4-oxadiazol 
• 95-54-5 1,2-diamino-benzene 
• 4970-61-0 5-amino-1,3,4-oxadiazole-2-carboxylic acid 
• 2302-84-3 1-formylthiosemicarbazide 
• 34005-36-2 carboxaldehyde semicarbazide 
• 4970-53-0 5-amino[1,3,4]oxadiazole-2-carboxylic acid ethyl ester 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 6694-34-4 1-[1,3,4]oxadiazol-2-yl-3-phenyl-urea 
• 69982-11-2 (triphenyl-λ⁵-phosphanylidene)-[1,3,4]oxadiazol-2-yl-amine 
• 1330128-61-4 4-[(2R)-1-(1,3,4-oxadiazol-2-ylamino)-1-oxopropan-2-yl]phenyl trifluoromethanesulfonate 

Relevant academic research and scientific papers

HETEROCYCLIC AMIDE COMPOUND

PROBLEM TO BE SOLVED: To provide a heterocyclic amide compound useful as an active ingredient of a herbicide. SOLUTION: The present disclosure provides a heterocyclic amide compound represented by the following formula or a salt thereof. Q-N(R3)-C(=X)-W (Q: a substituted/unsubstituted 1,3,4-oxadiazole, 1,2,5-oxadiazole or the like. W: a substituted/unsubstituted [1,2,4]triazolo[4,3-a]pyridine or the like. X: O, S. R3: H, C1-C6 alkyl or the like). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

HETEROCYCLIC AMIDE COMPOUND

PROBLEM TO BE SOLVED: To provide a herbicide that reliably has an effect on various weeds at a reduced dosage, has reduced trouble such as soil pollution and influence on succeeding crops, and is highly safe. SOLUTION: The present invention provides a heterocyclic amide compound represented by the following formula and a herbicide containing the same. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

HETEROCYCLIC AMIDO COMPOUND

PROBLEM TO BE SOLVED: To provide a novel pesticide, especially a herbicide. SOLUTION: There are provided a heterocycle amide compound such as 3-isopropyl-N-(5-methyl-1, 3, 4-oxadiazole-2-yl)-5-(trifluoromethyl)-[1, 2, 4]triazolo [4,3-a] pyridine-8-carboxamide (compound No.1-004), 3-isopropyl-N-(5-methyl-1, 3, 4-oxadiazole-2-yl)-5-(methylthio)-[1,2,4] triazolo [4,3-a] pyridine-8-carboxamide (compound No.1-009), and a herbicide containing them. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

The heterocyclic amide compound (by machine translation)

[Problem] an agrochemical, especially useful as a herbicide, the novel 1, 2, 4: triazolo 4,3-: pyridine-based compound. (1) the heterocyclic amide compound represented by the formula [a] and containing the herbicide. [Q may have a substituent can be an oxadiazole group, a tetrazole group, a triazole group, an oxazole group, an isoxazole group; W is a substituent group which may have 1, 2, 4: triazolo 4,3-: pyridine group][Drawing] no (by machine translation)

Studies on Decarboxylation Reactions. Part 5. Micellar Catalysis and Mixed Solvents Effects on the Decarboxylation of Some N-Alkyl- or N-Aryl-substituted 5-Amino-1,3,4-oxadiazole-2-carboxylic Acids

The effect of micelles and mixed solvents on the decarboxylation of some N-alkyl- or N-aryl-substituted 5-amino-1,3,4-oxadiazole-2-carboxylic acids has been studied.The data support the unimolecular decarboxylation mechanism proposed by us.Moreover, they show that mixed solvents and micelles have different effects on reactivity of the amino acids under study.

Studies on Decarboxylation Reactions. Part 6. Kinetic Study of Decarboxylation of 5-Amino-1,3,4-oxadiazole-2-carboxylic Acid and its N-Phenyl Derivatives at High Hydrochloric Acid Concentrations

The dissociation constants (K1) of both acids 4a-c and esters 5a-c and the rate constants of the decarboxylation reaction of acids 4a-c have been measured at various high concentrations of hydrochloric acid (0.5-8.0 M range).The results obtained have enabled us to suggest the probable structure of the zwitterion which undergoes decarboxylation.