17243-69-5 Usage
Description
Ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate is an amino acid ester that serves as the ethyl ester of cyclohex-3-ene-1-carboxylic acid. The cyclohexane ring in this compound is substituted at positions 1 and 2 by phenyl and dimethylamino groups, respectively. This molecule has four possible diastereoisomers, and the opioid analgesic drug tilidine is a racemate composed of the two trans diastereoisomers.
Uses
Used in Pharmaceutical Industry:
Ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate is used as an active pharmaceutical ingredient for the development of opioid analgesic drugs. Its diastereoisomers contribute to the formulation of tilidine, a medication used to treat moderate to severe pain. The compound's unique structure allows it to interact with opioid receptors in the central nervous system, providing pain relief.
Used in Research and Development:
In the field of medicinal chemistry and pharmaceutical research, ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate serves as a key compound for studying the structure-activity relationship of opioid analgesics. Its diastereoisomers can be investigated to understand their individual contributions to the overall pharmacological effects of tilidine, potentially leading to the development of more effective and safer pain management medications.
Used in Drug Synthesis:
Ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate is utilized as a synthetic intermediate in the production of various pharmaceutical compounds, particularly those with opioid activity. Its unique structure makes it a valuable building block for the synthesis of novel drugs with potential applications in pain management and other therapeutic areas.
Used in Quality Control and Standardization:
ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate is also employed in the quality control and standardization of pharmaceutical products containing tilidine or its derivatives. By analyzing the presence and比例 of the four possible diastereoisomers, manufacturers can ensure the consistency, potency, and safety of the final drug product.
Check Digit Verification of cas no
The CAS Registry Mumber 17243-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17243-69:
(7*1)+(6*7)+(5*2)+(4*4)+(3*3)+(2*6)+(1*9)=105
105 % 10 = 5
So 17243-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO2/c1-4-20-16(19)17(14-10-6-5-7-11-14)13-9-8-12-15(17)18(2)3/h5-8,10-12,15H,4,9,13H2,1-3H3
