372159-53-0 Usage
Uses
Used in Pharmaceutical Research:
(R)-tert-butyl 5-methoxychroman-3-ylcarbamate is used as a building block for the synthesis of novel bioactive molecules in the pharmaceutical industry. Its unique structural characteristics, including the chroman ring and carbamate group, contribute to its potential in creating new compounds with therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (R)-tert-butyl 5-methoxychroman-3-ylcarbamate is used as a starting point for designing and developing new drugs. The presence of the methoxy group on the chroman ring may confer specific pharmacological properties, making it a promising candidate for further study and potential use in the development of targeted therapeutics.
Used in Drug Development:
(R)-tert-butyl 5-methoxychroman-3-ylcarbamate is utilized as a key component in drug development, particularly for creating molecules with potential therapeutic effects. Its ability to interact with biological systems makes it a valuable asset in the search for new treatments and medications to address various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 372159-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,1,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 372159-53:
(8*3)+(7*7)+(6*2)+(5*1)+(4*5)+(3*9)+(2*5)+(1*3)=150
150 % 10 = 0
So 372159-53-0 is a valid CAS Registry Number.
372159-53-0Relevant academic research and scientific papers
Usse, Stephanie,Pave, Gregoire,Guillaumet, Gerald,Viaud-Massuard, Marie-Claude
, p. 1689 - 1694 (2001)
Enantiomerically pure (3R)-amino-5-methoxy-3,4-dihydro-2H-1-benzopyran was successfully synthesised in nine steps starting from L-serine. The same synthetic pathway was used to prepare the (3S)-aminochroman derivative starting from D-serine. The enantiomeric purity of the final aminochroman derivatives was determined by capillary electrophoresis using β-cyclodextrin as the chiral selector.
