69363-09-3 Usage
General Description
The chemical compound "(1S,2S,3R,5S)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol" is a bicyclic organic molecule with a three-dimensional structure. Its chemical formula is C10H19NO, and it contains an amino group and a hydroxyl group, making it an amino alcohol. The compound is chiral, exhibiting four stereocenters in its structure, denoted by the (1S,2S,3R,5S) prefix. (1S,2S,3R,5S)-3-Amino-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol is commonly used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure and stereochemistry make it a valuable intermediate in the preparation of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 69363-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,6 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69363-09:
(7*6)+(6*9)+(5*3)+(4*6)+(3*3)+(2*0)+(1*9)=153
153 % 10 = 3
So 69363-09-3 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-/m0/s1
69363-09-3Relevant articles and documents
COMPOUNDS, COMPOSITIONS AND METHODS FOR SYNTHESIS
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Paragraph 001613; 001614; 001617; 001618, (2019/01/10)
The present disclosure, among other things, provides technologies for synthesis, including reagents and methods for stereoselective synthesis. In some embodiments, the present disclosure provides compounds useful as chiral auxiliaries. In some embodiments, the present disclosure provides reagents and methods for oligonucleotide synthesis. In some embodiments, the present disclosure provides reagents and methods for chirally controlled preparation of oligonucleotides. In some embodiments, technologies of the present disclosure are particularly useful for constructing challenging internucleotidic linkages, providing high yields and stereoselectivity.
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.
