73657-24-6 Usage
Uses
Used in Scientific Research:
(1R,2S)-(+)-BORNYLAMINE HCL is used as an intermediate in the synthesis of more complex compounds or molecules. Its enantiomeric excess and role in stereospecific reactions make it a valuable compound for researchers in the field of chemistry and related disciplines.
Used in Stereospecific Reactions:
(1R,2S)-(+)-BORNYLAMINE HCL is used as a reactant in stereospecific reactions, where the mechanism allows for the stereoselective formation of specific isomers. This property is crucial for the development of enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and materials science.
Used in Laboratory Environments:
(1R,2S)-(+)-BORNYLAMINE HCL is used in laboratory settings for various experiments and studies. Its unique properties and potential applications make it an important compound for researchers to explore and understand its behavior and interactions with other compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 73657-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,5 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73657-24:
(7*7)+(6*3)+(5*6)+(4*5)+(3*7)+(2*2)+(1*4)=146
146 % 10 = 6
So 73657-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N.ClH/c1-9(2)7-4-5-10(9,3)8(11)6-7;/h7-8H,4-6,11H2,1-3H3;1H/t7?,8-,10-;/m0./s1
73657-24-6Relevant academic research and scientific papers
Synthesis of Optically Active Triazolinediones and Examination of Their Utility for Inducing Asymmetry in Diels-Alder Cycloaddition Reactions
Paquette, Leo A.,Doehner, Robert F.
, p. 5105 - 5113 (2007/10/02)
(S)-(-)-α-Methylbenzylamine, dehydroabietylamine, and endo-bornylamine have been transformed into the optically pure triazolinediones via the respective isocyanates and urazoles.Their ability to discriminate between diastereomeric Diels-Alder transition states was determined in the case of two dienes, 2,4-p-menthadiene and α-phellandrene, which were prepared in racemic and optically active forms of known enantiomeric purity.Exhaustive cycloaddition to these dienes gave the needed pairs of adduct D reference points against which those obtained in the asymmetric induction studies could be compared.By this technique, simple plots of D vs. diastereomeric purity served to delineate not only the level of enantioselection but also the absolute configuration of the adducts.Due in part to their exceptionally high reactivity, the triazolinediones are not sufficiently selective to permit high levels of enantioselection.Rather, their usefulness lies in their ability to achieve nondestructive resolution of various nonobivously resolvable compounds.
