10171-76-3 Usage
Uses
Used in Organic Synthesis:
(1R,4S)-N-[[(1S,4R)-Bicyclo[2.2.1]heptan-2α-yl]methyl]bicyclo[2.2.1]heptane-2β-methanamine is used as a key intermediate in organic synthesis for its unique structural features and potential reactivity. Its chiral nature and complex ring system may enable the development of novel compounds with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1R,4S)-N-[[(1S,4R)-Bicyclo[2.2.1]heptan-2α-yl]methyl]bicyclo[2.2.1]heptane-2β-methanamine is used as a building block for the development of new drugs. Its chirality and complex structure may offer advantages in the design of chiral drugs with improved selectivity and efficacy. Further research is needed to explore its potential as a pharmaceutical agent.
Used in Materials Science:
(1R,4S)-N-[[(1S,4R)-Bicyclo[2.2.1]heptan-2α-yl]methyl]bicyclo[2.2.1]heptane-2β-methanamine is utilized in materials science for its potential to contribute to the development of new materials with unique properties. Its complex ring system and primary amine functional group may enable the creation of materials with specific characteristics, such as enhanced stability, reactivity, or selectivity, depending on the application.
Check Digit Verification of cas no
The CAS Registry Mumber 10171-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10171-76:
(7*1)+(6*0)+(5*1)+(4*7)+(3*1)+(2*7)+(1*6)=63
63 % 10 = 3
So 10171-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H27N/c1-3-13-5-11(1)7-15(13)9-17-10-16-8-12-2-4-14(16)6-12/h11-17H,1-10H2
10171-76-3Relevant academic research and scientific papers
Colloid and nanosized catalysts in organic synthesis: XII. Hydrogenation of carbonitriles catalyzed by nickel nanoparticles
Mokhov,Popov,Shcherbakova
, p. 273 - 280 (2016/04/20)
Hydrogenation of carbonitriles catalyzed by nickel nanoparticles in isopropanol proceeds under atmospheric pressure of hydrogen within 6-15 h to yield mainly secondary amines. Hydrogenation of α-aminonitriles results in reductive decyanation. β-Aminonitriles undergo hydrogenolysis at the nitrogen-carbon bond.
