852227-91-9 Usage
Uses
Used in Organic Synthesis:
METHYL-(5-PHENYL-ISOXAZOL-3-YLMETHYL)-AMINE HYDROCHLORIDE is used as a building block for the synthesis of various organic compounds due to its unique structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, METHYL-(5-PHENYL-ISOXAZOL-3-YLMETHYL)-AMINE HYDROCHLORIDE is used as a precursor or intermediate in the development of new pharmaceuticals, potentially contributing to the creation of novel therapeutic agents.
Used in Drug Development:
METHYL-(5-PHENYL-ISOXAZOL-3-YLMETHYL)-AMINE HYDROCHLORIDE is utilized as a component in drug development processes, where its properties may be harnessed to enhance the efficacy, stability, or delivery of pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 852227-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,2,2 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 852227-91:
(8*8)+(7*5)+(6*2)+(5*2)+(4*2)+(3*7)+(2*9)+(1*1)=169
169 % 10 = 9
So 852227-91-9 is a valid CAS Registry Number.
852227-91-9Relevant academic research and scientific papers
Methylamine Derivatives with 1,2-Azole Fragments: Synthesis, Palladium Complexes, Catalysis of the Suzuki Reaction
Akishina, E. A.,Alekseyev, R. S.,Bumagin, N. A.,Dikusar, Е.А.,Petkevich, S. K.,Potkin, V. I.
, p. 1512 - 1518 (2021/09/11)
Abstract: New methylamine derivatives with 1,2-azole fragments (phenylisoxazole, p-tolylisoxazole, 2,5-dimethylphenylisoxazole and 4,5-dichloroisothiazole) and their palladium complexes were synthesized. It was shown that palladium complexes with the obta
Synthesis of 3-aminomethyl-substituted pyrazoles and isoxazoles
Musatov,Starodubtseva,Rakishev,Turova,Vinogradov
experimental part, p. 1199 - 1203 (2011/12/15)
A series of new 3-(aminomethyl)pyrazoles and 3-(aminomethyl)isoxazoles was synthesized along a route involving the formation as key intermediates of esters of 5-substituted 1H-pyrazole-3-carboxylic and 1H-isoxazole-3-carboxylic acids. All compounds obtain
