168286-10-0 Usage
General Description
(1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol, also known as norcamphorol, is a bicyclic compound with a unique structure. It contains an amino group, a hydroxyl group, and three methyl groups. (1R,2R,3S,5R)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is chiral, with four stereocenters, and exists as a mixture of enantiomers. Norcamphorol has potential applications in medicinal chemistry, as its bicyclic structure may offer interesting biological activities. The compound may also have utility as a building block in organic synthesis due to its interesting and complex structure. Further research on norcamphorol's properties and potential applications is warranted to fully understand its potential uses.
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 articles and documents
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.
, 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.
