28646-40-4 Usage
Uses
Used in Pharmaceutical Applications:
(-)-11-HYDROXY-DELTA8-TETRAHYDROCANNABINOL is used as a therapeutic agent for various medical conditions due to its potential analgesic, anti-inflammatory, and neuroprotective properties. It may be particularly useful in the treatment of chronic pain, inflammation, and neurodegenerative disorders.
Used in Research and Development:
(-)-11-HYDROXY-DELTA8-TETRAHYDROCANNABINOL serves as a valuable compound for scientific research, particularly in the fields of pharmacology, neuroscience, and drug development. Its study can provide insights into the mechanisms of action of cannabinoids and their potential applications in medicine.
Used in the Cannabis Industry:
In the cannabis industry, (-)-11-HYDROXY-DELTA8-TETRAHYDROCANNABINOL is used as a component in the development of new cannabis products with potentially enhanced therapeutic effects. Its unique properties may contribute to the creation of novel formulations and delivery methods for medical and recreational use.
Used in Toxicology Studies:
(-)-11-HYDROXY-DELTA8-TETRAHYDROCANNABINOL is also utilized in toxicology research to better understand the safety and potential side effects of cannabis consumption. This knowledge can help inform regulations, guidelines, and consumer education regarding the responsible use of cannabis products.
Check Digit Verification of cas no
The CAS Registry Mumber 28646-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28646-40:
(7*2)+(6*8)+(5*6)+(4*4)+(3*6)+(2*4)+(1*0)=134
134 % 10 = 4
So 28646-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O3/c1-4-5-6-7-14-11-18(23)20-16-10-15(13-22)8-9-17(16)21(2,3)24-19(20)12-14/h8,11-12,16-17,22-23H,4-7,9-10,13H2,1-3H3/t16-,17-/m1/s1
28646-40-4Relevant articles and documents
The synthesis of some 11-substituted tetrahydrocannabinol metabolites
ApSimon, John W.,Collier, T. Lee,Guiver, Michael D.
, p. 2804 - 2809 (2007/10/02)
9-Bromo-11-oxo-hexahydrocannabinol (5) was prepared from the ketocannabinoid 3b via the epoxysulfone 4.The dehydrobromination of the bromoaldehyde 5 could be controlled to give either the thermodinamically more stable Δ8-aldehyde 2c, or the Δ9-aldehyde 1c by an intramolecularly assisted elimination.Reduction of the unsaturated aldehydes gave the allylic alcohol metabolites 2a and 1a, respectively.