27916-82-1 Usage
Uses
Used in Pharmaceutical Industry:
2,3-dihydro-1-benzothiophene-2-carboxylic acid (SALTDATA: FREE) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3-dihydro-1-benzothiophene-2-carboxylic acid (SALTDATA: FREE) serves as a crucial building block for the creation of novel agrochemicals. Its incorporation into these compounds can lead to the development of more effective and environmentally friendly pesticides, herbicides, and other agricultural products.
Used in Organic Synthesis:
2,3-dihydro-1-benzothiophene-2-carboxylic acid (SALTDATA: FREE) is utilized as a versatile building block in organic synthesis. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of organic compounds, including specialty chemicals, dyes, and other materials with diverse applications.
Used in Chemical Research:
As a chemical compound with a distinctive structure, 2,3-dihydro-1-benzothiophene-2-carboxylic acid (SALTDATA: FREE) is employed in various chemical research applications. It is used to study reaction mechanisms, explore new synthetic routes, and investigate the properties of related compounds, furthering our understanding of organic chemistry and its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 27916-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,1 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27916-82:
(7*2)+(6*7)+(5*9)+(4*1)+(3*6)+(2*8)+(1*2)=141
141 % 10 = 1
So 27916-82-1 is a valid CAS Registry Number.
27916-82-1Relevant 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.
