39192-51-3 Usage
Uses
Used in Research and Development:
1-(3,5-DIMETHOXYPHENYL)HEPTAN-1-ONE 96 is used as a research compound for exploring its chemical properties, reactivity with other substances, and potential applications in various fields. Its unique structure and purity make it valuable for scientific investigations and the development of new chemical processes or products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(3,5-DIMETHOXYPHENYL)HEPTAN-1-ONE 96 may be used as an intermediate or building block in the synthesis of various pharmaceutical compounds. Its aromatic ketone nature and dimethoxyphenyl group could contribute to the development of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
1-(3,5-DIMETHOXYPHENYL)HEPTAN-1-ONE 96 can be employed as a key component in the synthesis of other organic compounds, particularly those with similar structural features. Its reactivity and functional groups make it a versatile starting material for the production of various chemical products.
Used in Material Science:
In material science, 1-(3,5-DIMETHOXYPHENYL)HEPTAN-1-ONE 96 may have potential applications in the development of new materials with specific properties, such as improved stability, reactivity, or other characteristics. Its unique structure could contribute to the creation of novel materials with potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 39192-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39192-51:
(7*3)+(6*9)+(5*1)+(4*9)+(3*2)+(2*5)+(1*1)=133
133 % 10 = 3
So 39192-51-3 is a valid CAS Registry Number.
39192-51-3Relevant academic research and scientific papers
Synthesis of functionalized cannabinoids
Harrington, Paul E.,Stergiades, Ioanna A.,Erickson, Joy,Makriyannis, Alexandros,Tius, Marcus A.
, p. 6576 - 6582 (2007/10/03)
An effective synthesis of tricyclic, nonclassical cannabinoids has been developed on the basis of a cation-olefin cyclization that forms the two nonaromatic rings with the desired stereochemistry in a single step.
Pharmacophoric requirements for cannabinoid side chains: Multiple bond and C1'-substituted Δ8-tetrahydrocannabinols
Papahatjis,Kourouli,Abadji,Goutopoulos,Makriyannis
, p. 1195 - 1200 (2007/10/03)
Accumulated evidence indicates that within the cannabinoid structure the aliphatic side chain plays a pivotal role in determining cannabimimetic activity. We describe the synthesis and affinities for the CB1 and CB2 receptors of a series of novel Δ8
