88230-53-9 Usage
Uses
Used in Pharmaceutical Industry:
N-(furan-2-ylmethyl)butan-1-amine is utilized as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure allows it to serve as a building block in the creation of novel drug molecules, potentially leading to the development of new treatments for a range of medical conditions.
Used in Drug Development:
In the realm of drug development, N-(furan-2-ylmethyl)butan-1-amine is employed as a key component in the design and synthesis of innovative pharmaceutical agents. Its presence in a compound may contribute to desired biological activities, such as binding affinity to specific targets or modulation of cellular pathways, which are crucial for therapeutic efficacy.
Used in Organic Synthesis:
N-(furan-2-ylmethyl)butan-1-amine also finds application in organic synthesis, where it can be used to create a variety of complex organic molecules. Its versatility in forming different types of chemical bonds and its compatibility with various synthetic routes make it a valuable tool for chemists working on the development of new organic compounds.
The specific applications and uses of N-(furan-2-ylmethyl)butan-1-amine will depend on further research and testing to fully understand its properties and potential interactions within biological systems. As with any chemical compound, its successful integration into pharmaceutical products or other applications will require rigorous evaluation and optimization.
Check Digit Verification of cas no
The CAS Registry Mumber 88230-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88230-53:
(7*8)+(6*8)+(5*2)+(4*3)+(3*0)+(2*5)+(1*3)=139
139 % 10 = 9
So 88230-53-9 is a valid CAS Registry Number.
88230-53-9Relevant academic research and scientific papers
Catalytic Hydroamination of Furfuryl and Tetrahydrofurfuryl Alcohols with Nitriles
Kozintsev, S. I.,Basalaeva, L. I.,Gladkikh, L. V.,Kozlov, N. S.
, p. 19 - 21 (2007/10/02)
Reaction of furfuryl and tetrahydrofurfuryl alcohols with nitriles over copper oxide catalysts under a hydrogen pressure of 15 atm at a temperature of 230 deg C gives N-alkylfurfuryl- (yield 46-50percent) and N-alkyltetrahydrofurfurylamines (49-53percent), and N-alkylpiperidines (28-41percent).A reaction mechanism is proposed.
