925252-83-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(1-NAPHTHYL)ACETAMIDOXIME is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its ability to inhibit the activity of certain enzymes makes it a valuable component in the development of new treatments for various medical conditions.
Used in Antioxidant Applications:
2-(1-NAPHTHYL)ACETAMIDOXIME is used as an antioxidant in the development of new drugs or treatments for various medical conditions. Its antioxidant properties can help protect cells from damage caused by reactive oxygen species and may contribute to the prevention or treatment of diseases associated with oxidative stress.
Check Digit Verification of cas no
The CAS Registry Mumber 925252-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,2,5 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 925252-83:
(8*9)+(7*2)+(6*5)+(5*2)+(4*5)+(3*2)+(2*8)+(1*3)=171
171 % 10 = 1
So 925252-83-1 is a valid CAS Registry Number.
925252-83-1Relevant articles and documents
Synthesis of 4,5-dihydro 1,2,4-oxadiazoles from N-unsubstituted amidoximes
Lessel,Herfs
, p. 22 - 26 (2007/10/03)
4,5-Dihydro 1,2,4-oxadiazoles can be synthesized from aromatic and araliphatic amidoximes by cyclocondensation with aldehydes and ketones. Resulting heterocycles differ in substitution at C-3 and C-5 showing the scope of the simple reaction.
Discovery of potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70
Vu, Chi B.,Corpuz, Evelyn G.,Merry, Taylor J.,Pradeepan, Selvaluxmi G.,Bartlett, Catherine,Bohacek, Regine S.,Botfield, Martyn C.,Eyermann, Charles J.,Lynch, Berkley A.,MacNeil, Ian A.,Ram, Mary K.,Van Schravendijk, Marie Rose,Violette, Shelia,Sawyer, Tomi K.
, p. 4088 - 4098 (2007/10/03)
A series of 1,2,4-oxadiazole analogues has been shown to be potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70, a potential therapeutic target for immune suppression. These compounds typically are 200- 400-fold more potent than the native,