654680-82-7 Usage
Description
(1R,3R,4S,6S)-4-AMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPT-3-YL-METHANOL is a chemical compound with a unique bicyclic structure. It features a hydroxyl group attached to a bicyclic heptane ring, with methyl groups at the 4th and 7th carbon positions, and an amino group at the 4th carbon position. (1R,3R,4S,6S)-4-AMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPT-3-YL-METHANOL may have potential pharmaceutical applications due to its distinctive structure and functional groups, but further research is necessary to fully explore its properties and potential uses.
Uses
Used in Pharmaceutical Industry:
(1R,3R,4S,6S)-4-AMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPT-3-YL-METHANOL is used as a potential pharmaceutical candidate for various applications due to its unique structure and functional groups. Its potential uses may include the development of new drugs or therapies, targeting specific diseases or conditions. Further research is needed to fully understand its properties and potential applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 654680-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,6,8 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 654680-82:
(8*6)+(7*5)+(6*4)+(5*6)+(4*8)+(3*0)+(2*8)+(1*2)=187
187 % 10 = 7
So 654680-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO/c1-10(2)8-4-7(6-13)11(3,12)5-9(8)10/h7-9,13H,4-6,12H2,1-3H3/t7-,8+,9-,11-/m0/s1
654680-82-7Relevant articles and documents
Synthesis of new chiral schiff bases from (+)-3-carene and their use in asymmetric oxidation of sulfides catalyzed by metal complexes
Koneva,Volcho,Korchagina,Salakhutdinov,To
experimental part, p. 815 - 824 (2009/12/09)
A number of new chiral Schiff bases were synthesized starting from accessible monoterpene (+)-3-carene, and the products were used as ligands in metal complex-catalyzed oxidation of sulfides to chiral sulfoxides. The optical purity and the sign of optical rotation of chiral sulfoxides were found to strongly depend on the oxidation temperature. Pleiades Publishing, Ltd., 2009.