56674-68-1 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(Cyclohexyloxy)propanoic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of drugs for an array of medical conditions. Its chemical versatility allows for the creation of new compounds with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, 2-(Cyclohexyloxy)propanoic acid is employed as a valuable precursor, facilitating the synthesis of a wide range of organic compounds. Its structural attributes make it an essential component in the construction of complex molecules for both research and industrial purposes.
Used in Drug Development:
2-(Cyclohexyloxy)propanoic acid is harnessed in the development of new drugs, serving as a crucial building block in the formulation of potential therapeutic agents. Its role in the creation of novel compounds with medicinal properties underscores its importance in advancing pharmaceutical research and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 56674-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56674-68:
(7*5)+(6*6)+(5*6)+(4*7)+(3*4)+(2*6)+(1*8)=161
161 % 10 = 1
So 56674-68-1 is a valid CAS Registry Number.
56674-68-1Relevant academic research and scientific papers
Further structure-activity relationships in the series of tropanyl esters endowed with potent antinociceptive activity
Scapecchi, Serena,Giorgi, Antonella,Bellucci, Cristina,Dei, Silvia,Ghelardini, Carla,Manetti, Dina,Romanelli, M. Novella,Teodori, Elisabetta
, p. 764 - 772 (2007/10/03)
Several analogs of the α-tropanyl esters of 2-(4-chlorophenoxy)butyric acid (SM21) and 2-phenylthiobutyric acid (SM32), endowed with potent antinociceptive and cognition enhancing activity, were synthesized, aimed at obtaining more potent and safe drug candidates. Variation of the acyl moiety, as well as the conformational restriction of atropine to give the α-tropanyl ester of 2,3-dihydrobenzofurane-3-carboxylic acid (18), practically abolished activity. In the case of 18, the antimuscarinic activity was also severely affected by the conformation restrain. On the contrary, conformational restriction of phenoxybutyric and phenylthiobutyric acid derivatives to give the α-tropanyl ester of 2,3-dihydro-benzofurane-2-carboxylic acid and 2,3-dihydro-benzothiophene-2-carboxylic acid, afforded potent analgesic drugs that unfortunately were too toxic to be reliable drug candidates. A series of related esters of benzofurane-3-carboxylic acid and benzothiophene-3-carboxylic acid were also studied and found to be potent but toxic analgesics.
