37384-61-5 Usage
General Description
Methyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate is a chemical compound with the formula C11H8N2O3. It is a white to yellow crystalline powder that is used in the synthesis of pharmaceuticals and agrochemicals. METHYL 5-PHENYL-1,2,4-OXADIAZOLE-3-CARBOXYLATE has potential use in the development of new drugs due to its bioactivity and pharmacological properties. It is also a building block in the production of other organic compounds, particularly in the field of medicinal chemistry. Additionally, methyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate has been studied for its potential applications in materials science, such as in the development of new polymers and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 37384-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,3,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37384-61:
(7*3)+(6*7)+(5*3)+(4*8)+(3*4)+(2*6)+(1*1)=135
135 % 10 = 5
So 37384-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O3/c1-14-10(13)8-11-9(15-12-8)7-5-3-2-4-6-7/h2-6H,1H3
37384-61-5Relevant articles and documents
Acid-promoted reaction of N-(cyanomethyl) amide with nitrosation reagent: Facile synthesis of 1,2,4-oxadiazole-3-carboxamide
Du, Shaoqing,Fu, Wen,Li, Jin,Qian, Xuhong,Shao, Xusheng,Xu, Xiaoyong
supporting information, (2021/06/15)
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
Nitrosation of methyl 2-acylamino-3-dimethylaminopropenoates. A simple conversion of N-acylglycines into 5-substituted 1,2,4-oxadiazole-3-carboxylates
Kmetic,Stanovnik
, p. 1563 - 1565 (2007/10/03)
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
