76793-01-6 Usage
Description
(1R,4R,5S,6S)-1,3,3-trimethyl-6-(pyrrolidin-1-yl)-2-oxabicyclo[2.2.2]octan-5-ol is a complex bicyclic organic compound with a unique molecular structure. It features a five-membered ring with an additional oxygen atom, a pyrrolidine ring, and a hydroxyl group. As a chiral molecule with four stereocenters, it can exist in multiple stereoisomeric forms. The presence of the pyrrolidine moiety, a common structural element in many pharmaceuticals and natural products, suggests that this compound may have biological activity and potential medicinal applications. Its structure also hints at possible involvement in neurological or physiological processes.
Uses
Used in Pharmaceutical Industry:
(1R,4R,5S,6S)-1,3,3-trimethyl-6-(pyrrolidin-1-yl)-2-oxabicyclo[2.2.2]octan-5-ol is used as a potential pharmaceutical candidate due to its complex structure and the presence of the pyrrolidine moiety, which is commonly found in many drugs and natural products with medicinal properties.
Used in Neurological Applications:
Given the presence of the pyrrolidine ring and the hydroxyl group, (1R,4R,5S,6S)-1,3,3-trimethyl-6-(pyrrolidin-1-yl)-2-oxabicyclo[2.2.2]octan-5-ol may be used in the development of treatments for neurological disorders, as its structure suggests potential involvement in neurological processes.
Used in Physiological Research:
(1R,4R,5S,6S)-1,3,3-trimethyl-6-(pyrrolidin-1-yl)-2-oxabicyclo[2.2.2]octan-5-ol's structure, with its potential impact on physiological processes, makes (1R,4R,5S,6S)-1,3,3-trimethyl-6-(pyrrolidin-1-yl)-2-oxabicyclo[2.2.2]octan-5-ol a candidate for research into physiological mechanisms and the development of therapies targeting various physiological conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 76793-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76793-01:
(7*7)+(6*6)+(5*7)+(4*9)+(3*3)+(2*0)+(1*1)=166
166 % 10 = 6
So 76793-01-6 is a valid CAS Registry Number.
76793-01-6Relevant articles and documents
Carbonyl Transposition and Regio- and Stereo-specific Syntheses of New Alcohols, Amino-alcohols, and Ketones in the Monoterpenoid 1,3,3-Trimethyl-2-oxabicyclooctane
Bondavalli, Francesco,Schenone, Pietro,Ranise, Angelo,Lanteri, Silvia
, p. 2626 - 2630 (2007/10/02)
An efficient transposition of carbonyl group R1-CO-CH2-R2 -> R1-CH2-CO-R2 in the 1,3,3-trimethyl-2-oxabicyclooctane system was carried out via hydroboration-oxidation of 6-dialkylamino-1,3,3-trimethyl-2-oxabicyclooct-5-enes (3a-c), which gave regio- and stereo-specifically 6-cis-dialkylamino-1,3,3-trimethyl-2-oxabicyclooctan-5-trans-ols (4a-c) in high yield.Cope reaction on the N-oxide (5b) obtained from the amino-alcohol (4b) with hydrogen peroxide led to 1,3,3-trimethyl-2-oxabicyclooctan-5-one (6), the other possible isomer of the long-known 1,3,3-trimethyl-2-oxabicyclooctan-6-one (1b).The ketone (6) was also obtained from 1,3,3-trimethyl-2-oxabicyclooct-5-ene (2) via its trans-epoxide (11), lithium aluminium hydride reduction at 160-165 deg C of which gave stereo- and regio-specifically 1,3,3-trimethyl-2-oxabicyclooctan-5-trans-ol (9b).Chromic acid oxidation of (9b) and (4a-c) under various conditions gave the ketone (6) and the amino-ketones (7a-c), respectively.Lithium aluminium hydride reduction of (6) and (7a-c) afforded stereospecifically the cis-alcohol (9a) and 6-cis-dialkylamino-1,3,3-trimethyl-2-oxabicyclooctan-5-cis-ols (8a-c), respetively.Hydroboration-oxidation of the alkene (2) was not regiospecific, giving a 3:1 mixture of the trans-alcohols (9b) and (10b), respectively.