98421-28-4 Usage
Uses
Used in Pharmaceutical Industry:
2-(quinolin-5-yl)ethanamine is used as a key intermediate in the synthesis of various drugs for its ability to contribute to the development of new therapeutic agents. Its presence in drug molecules can enhance their pharmacological profiles, making it a valuable component in the creation of medications with improved efficacy and safety.
Used in Chemical Industry:
In the chemical industry, 2-(quinolin-5-yl)ethanamine serves as a precursor for the production of biologically active molecules, which can be further utilized in research and development for potential applications in medicine and other fields. Its reactivity and structural features make it a suitable candidate for the creation of complex organic compounds.
Used in Medicinal Chemistry Research:
2-(quinolin-5-yl)ethanamine is used as a research compound for exploring its antihistaminic, antiallergic, and antipsychotic properties. This allows scientists to investigate its potential as a therapeutic agent for various conditions, including allergies and mental health disorders, thereby contributing to the advancement of treatment options.
Used in Drug Development:
2-(quinolin-5-yl)ethanamine is utilized in drug development as a structural component that can influence the pharmacokinetics and pharmacodynamics of new drug candidates. Its incorporation into drug molecules can lead to the discovery of drugs with better absorption, distribution, metabolism, excretion, and toxicity profiles, which are crucial for successful clinical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 98421-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,2 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98421-28:
(7*9)+(6*8)+(5*4)+(4*2)+(3*1)+(2*2)+(1*8)=154
154 % 10 = 4
So 98421-28-4 is a valid CAS Registry Number.
98421-28-4Relevant academic research and scientific papers
Kaiser, Carl,Dandrige, Penelope A.,Garvey, Eleanor,Flaim, Kathryn E.,Zeid, Robert L.,Hieble, J. Paul
, p. 1803 - 1810 (1985)
The potency of β-adrenoreceptor agonists, e.g.,isoproterenol, is strikingly increased by substitution of the meta catecholic hydroxyl group with the NH group of a carbostyril system.To explore the possibility that comparable potency enhacement might occur
