37384-61-5

Usage

Uses

Used in Pharmaceutical Industry:
METHYL 5-PHENYL-1,2,4-OXADIAZOLE-3-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for its bioactivity and pharmacological properties. It contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
METHYL 5-PHENYL-1,2,4-OXADIAZOLE-3-CARBOXYLATE is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in protecting crops and controlling pests.
Used in Medicinal Chemistry:
METHYL 5-PHENYL-1,2,4-OXADIAZOLE-3-CARBOXYLATE is used as a versatile building block in the production of other organic compounds, particularly in the field of medicinal chemistry. Its unique structure allows for the creation of diverse molecules with potential therapeutic applications.
Used in Materials Science:
METHYL 5-PHENYL-1,2,4-OXADIAZOLE-3-CARBOXYLATE is used in the development of new polymers and advanced materials. Its properties make it a valuable component in the creation of materials with improved performance characteristics for various applications.

InChI:InChI=1/C10H8N2O3/c1-14-10(13)8-11-9(15-12-8)7-5-3-2-4-6-7/h2-6H,1H3

Upstream product

• 5437-67-2 dimethyl 2-nitromalonate 
• 100-47-0 benzonitrile 
• 67-56-1 methanol 
• 5692-27-3 2-benzamido-ethanenitrile 
• 56952-04-6 methyl 2-N-benzoylamino-3-N,N-dimethylamino-2-propenoate 
• 125008-68-6 methyl (Z)-2-benzoylamino-3-dimethylaminopropenoate 

Downstream Products

• 1383581-74-5 N-hydroxy-5-phenyl-1,2,4-oxadiazole-3-carboxamide 
• 37937-62-5 5-phenyl-1,2,4-oxadiazole-3-carboxylic acid 

Relevant academic research and scientific papers

Acid-promoted reaction of N-(cyanomethyl) amide with nitrosation reagent: Facile synthesis of 1,2,4-oxadiazole-3-carboxamide

1,2,4-Oxadiazole-3-carboxamide has been extensively used in the pharmaceutical chemistry. In this study, 1,2,4-oxadiazole-3-carboxamide is accomplished through an acid-promoted reaction of N-(cyanomethyl)amide with nitrosation reagent. This novel preparat

Hydroxamic Acids as Potent Inhibitors of FeII and MnII E. coli Methionine Aminopeptidase: Biological Activities and X-ray Structures of Oxazole Hydroxamate-EcMetAP-Mn Complexes

New series of acids and hydroxamic acids linked to five-membered heterocycles including furan, oxazole, 1,2,4- or 1,3,4-oxadiazole, and imidazole were synthesized and tested as inhibitors against the FeII, CoII, and MnII f

Nitrosation of methyl 2-acylamino-3-dimethylaminopropenoates. A simple conversion of N-acylglycines into 5-substituted 1,2,4-oxadiazole-3-carboxylates

A novel simple synthesis of 5-substituted-1,2,4-oxadiazole-3-carboxylates 5 from N-acylglycines 1, which are transformed with DMF in the presence of phosphorus oxychloride into 2-substituted-4-dimethylaminomethyleneoxazol-5(4H)-ones 2, followed by opening

A New Synthetic Method of Alkyl Carbonocyanidate N-Oxides

A thermal decomposition of dimethyl nitromalonate to bis(carbomethoxy)furoxan was observed at about 170 deg C.In the presence of dipolarophiles, an intermediate, methyl carbonocyanidate N-oxide MeOCOCN->O, could be trapped as cycloadducts in good yields b