168286-10-0 Usage
Uses
Used in Medicinal Chemistry:
(1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is used as a pharmaceutical candidate for its potential biological activities. Its unique bicyclic structure may contribute to its efficacy in treating various medical conditions.
Used in Organic Synthesis:
(1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is used as a building block in organic synthesis for its interesting and complex structure. This allows for the creation of new compounds with potential applications in various industries.
Used in Chiral Chemistry:
(1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is used as a chiral compound in the development of enantioselective reactions and the synthesis of enantiomerically pure compounds. Its four stereocenters provide opportunities for exploring the effects of stereochemistry on biological activity and reactivity.
Used in Research:
(1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is used as a subject of research to further understand its properties and potential applications. This includes investigating its interactions with biopolymers and macromolecules, as well as its potential use in drug delivery systems and other therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 168286-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,2,8 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 168286-10:
(8*1)+(7*6)+(6*8)+(5*2)+(4*8)+(3*6)+(2*1)+(1*0)=160
160 % 10 = 0
So 168286-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H19NO/c1-9(2)6-4-7(9)10(3,12)8(11)5-6/h6-8,12H,4-5,11H2,1-3H3/t6-,7-,8+,10-/m1/s1
168286-10-0Relevant academic research and scientific papers
New chiral ligands derived from (+) and (-)-α-pinene for the enantioselective addition of diethylzinc to aldehydes
Frensch, Gustavo,Labes, Ricardo,Wosch, Celso Luiz,Munaretto, Laieli Dos Santos,Salomé, Kahlil Schwanka,Guerrero, Palimécio G.,Marques, Francisco A.
supporting information, p. 420 - 422 (2016/01/12)
In this study, we synthesized five new chiral ligands from (+) and (-)-α-pinene, which were successfully employed in the stereoselective addition of diethylzinc to aldehydes, leading to secondary chiral alcohols in up to 99% yield and 94% e.e.
A practical method for preparation of optically pure oxazaborolidines from α-pinene
Masui, Moriyasu,Shioiri, Takayuki
, p. 8363 - 8370 (2007/10/02)
(1S,2S,3R,5S)- and (1S,2S,3R,5S)-3-amino-2-hydroxypinane (1 and 2) were prepared from the corresponding α-pinene in optically pure form. They and their derivatives reacted with various organoborane compounds. A variety of chiral oxazaborolidines 3a-e and 4 were obtained in high yield.
