351166-64-8 Usage
Molecular weight
186.12 g/mol
The mass of one mole of the compound is 186.12 grams.
Ester derivative
1,2,5-oxadiazole-3-carboxylic acid
The compound is derived from 1,2,5-oxadiazole-3-carboxylic acid by forming an ester linkage.
Amino group
Contains an amino group (-NH2)
The presence of an amino group provides additional reactivity and potential for further chemical modifications.
Oxide group
Contains an oxide group (-O)
The presence of an oxide group may affect the compound's reactivity and stability.
Potential applications
Pharmaceutical and agricultural industries
The compound may be used in the development of new drugs and agrochemicals.
Biological activity
Oxadiazole ring
The presence of the oxadiazole ring suggests that the compound may have biological activity and could be used as a building block for the synthesis of biologically active compounds.
Stability
Stable compound
The compound's stability makes it suitable for further research and development.
Reactivity
Reactive molecule
The compound's reactivity allows for further chemical modifications and the synthesis of new compounds.
Research and development
Medicinal and agricultural chemistry
The compound's properties make it a valuable molecule for research and development in the fields of medicinal and agricultural chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 351166-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,1,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 351166-64:
(8*3)+(7*5)+(6*1)+(5*1)+(4*6)+(3*6)+(2*6)+(1*4)=128
128 % 10 = 8
So 351166-64-8 is a valid CAS Registry Number.
351166-64-8Relevant articles and documents
Straightforward Access to the Nitric Oxide Donor Azasydnone Scaffold by Cascade Reactions of Amines
Zhilin, Egor S.,Bystrov, Dmitry M.,Ananyev, Ivan V.,Fershtat, Leonid L.,Makhova, Nina N.
supporting information, p. 14284 - 14289 (2019/11/11)
A novel one-pot cascade method for the assembly of valuable NO-donor azasydnone scaffold has been developed. The construction strategy involves a diazotization/azo coupling/elimination/double rearrangement cascade sequence of readily available amines. The
