171007-01-5 Usage
Class
Oxadiazole compounds
The compound belongs to a class of heterocyclic compounds characterized by a five-membered ring containing oxygen and nitrogen atoms.
Structural features
Five-membered heterocyclic ring with oxygen and nitrogen atoms
The unique arrangement of atoms in the ring structure contributes to the compound's potential biological and chemical properties.
Potential applications
Building block in the synthesis of pharmaceuticals, agrochemicals, and materials
Due to its unique structure, the compound may be used as a starting point for creating various products in different industries.
Biological and chemical properties
Interesting properties due to its unique structure
The compound's structural features may lead to the discovery of new and useful properties, making it of interest to researchers in various fields.
Research significance
Development of new and useful products for various industries
Further investigation into the compound's properties and potential applications may result in the creation of innovative products for pharmaceuticals, agrochemicals, and materials science.
Synonym
1,2,4-Oxadiazol-3-amine, 5-butyl-(9CI)
This is an alternative name for the compound, which may be used in different contexts or databases.
Check Digit Verification of cas no
The CAS Registry Mumber 171007-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,0 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 171007-01:
(8*1)+(7*7)+(6*1)+(5*0)+(4*0)+(3*7)+(2*0)+(1*1)=85
85 % 10 = 5
So 171007-01-5 is a valid CAS Registry Number.
171007-01-5Relevant academic research and scientific papers
A generalized and efficient synthesis of 3-amino-, 3-(N-alkylamino)-, 3-(N,N-dialkylamino)-5-alkyl-1,2,4-oxadiazoles by irradiation of 3-alkanoylamino-4-phenyl-1,2,5-oxadiazoles (Furazans)
Buscemi,Vivona,Caronna
, p. 917 - 919 (2007/10/02)
Irradiation of 3-alkanoylamino-4-phenyl-1,2,5-oxadiazoles (furazans) at λ = 310 nm in methanol and in the presence of ammonia, primary or secondary aliphatic amines produced excellent yields of 3-amino-, 3-(N-alkylamino)-, 3-(N,N-dialkylamino)-5-alkyl-1,2
