497853-95-9 Usage
Uses
Used in Pharmaceutical Research:
(4-AMINOPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANOL is used as a molecular structure for pharmaceutical research and drug development due to the presence of the amino group and imidazole moiety, which are common functional groups in many pharmaceuticals.
Used in Drug Development:
(4-AMINOPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANOL is used as a potential candidate in drug development, as its specific properties and applications would depend on its synthesis, purity, and further research to fully understand its potential uses.
Used in Chemical Synthesis:
(4-AMINOPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANOL is used as a building block in chemical synthesis for creating new compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Used in Material Science:
(4-AMINOPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANOL is used as a component in material science for the development of new materials with specific properties, such as improved stability, reactivity, or selectivity in various applications.
Used in Agrochemicals:
(4-AMINOPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANOL is used as a starting material or intermediate in the synthesis of agrochemicals, such as pesticides or herbicides, due to its unique molecular structure and potential reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 497853-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,8,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 497853-95:
(8*4)+(7*9)+(6*7)+(5*8)+(4*5)+(3*3)+(2*9)+(1*5)=229
229 % 10 = 9
So 497853-95-9 is a valid CAS Registry Number.
497853-95-9Relevant academic research and scientific papers
BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE
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Page 236-237, (2010/02/06)
The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.
