CAS 105400-81-5
:(1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-ACETIC ACID
Description:
(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid is a chemical compound characterized by its unique structure, which includes a tetrahydroisoquinoline moiety linked to an acetic acid functional group. This compound typically exhibits properties associated with both isoquinoline derivatives and carboxylic acids, such as moderate solubility in polar solvents and potential biological activity. The presence of the tetrahydroisoquinoline structure suggests that it may interact with various biological targets, making it of interest in medicinal chemistry. Its acetic acid component contributes to its acidity and potential for forming salts or esters. The compound may also participate in various chemical reactions, including esterification and amidation, due to the presence of the carboxylic acid group. Overall, (1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetic acid is a versatile compound with potential applications in pharmaceuticals and organic synthesis, although specific biological activities and applications would require further investigation.
Formula:C11H13NO2
InChI:InChI=1/C11H13NO2/c13-11(14)7-10-9-4-2-1-3-8(9)5-6-12-10/h1-4,10,12H,5-7H2,(H,13,14)/t10-/m1/s1
SMILES:c1ccc2c(c1)CCN[C@@H]2CC(=O)O
Synonyms:- Rarechem Ak Ml 0229
- Timtec-Bb Sbb003633
- 1,2,3,4-Tetrahydroisoquinoline-1-Acetic Acid
- 2-(1,2,3,4-Tetrahydro-1-Isoquinolinyl)Acetic Acid
- Akos Bbs-00001341
- Iflab-Bb F1921-0016
- 1,2,3,4-Tetrahydroisoquinoline-1-Acetic Acid 98%
- (1S)-1,2,3,4-tetrahydroisoquinolinium-1-ylacetate
- (1R)-1,2,3,4-tetrahydroisoquinolinium-1-ylacetate
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Found 3 products.
(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid
CAS:Formula:C11H13NO2Purity:%Color and Shape:SolidMolecular weight:191.2264(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid
CAS:<p>(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid</p>Purity:≥95%Molecular weight:191.23g/mol(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid
CAS:<p>(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetic acid is a chemical compound that belongs to the esters family. It is enzymatically hydrolyzed by lipase and reactivity depends on the concentration of unreacted (1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetic acid. The ester reacts with methoxyethyl chloride via displacement of the chloride group by an alcohol group in the presence of base to produce (1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetate. This reaction is enantioselective and produces two enantiomers. The hydrolysis of the ester group occurs at a higher rate than that of the acetate group due to its lower polarity.</p>Formula:C11H13NO2Purity:Min. 95%Molecular weight:191.23 g/mol


