(S)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic acid

Product Name (S)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic acid
CAT No. CS-MM-50763
CAS No. 151004-92-1
Category Impurities
Stock IN-Stock
Mol. Wt. 177.2 g/mol
Mol. For. C10H11NO2
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles C1CNC(C2=CC=CC=C21)C(=O)O
InchIKey OXFGRWIKQDSSLY-VIFPVBQESA-N
Inchl InChI=1S/C10H11NO2/c12-10(13)9-8-4-2-1-3-7(8)5-6-11-9/h1-4,9,11H,5-6H2,(H,12,13)/t9-/m0/s1
IUPAC (1S)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
Controlled No
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(S)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic acid is a chemical compound that belongs to the class of heterocyclic compounds known as tetrahydroisoquinolines. It is an optically active molecule that exists in two enantiomeric forms, (R) and (S). The (S)-enantiomer is the biologically active form of the compound and is widely used in medicinal chemistry. The compound has been found to exhibit a range of biological activities, including anti-inflammatory, analgesic, and anticonvulsant effects. It has also been shown to modulate the activity of certain neurotransmitters, such as dopamine and serotonin, making it a potential target for the treatment of neurological disorders. In terms of chemical structure, (S)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic acid contains a ring system consisting of a six-membered ring fused to a five-membered ring. It also contains a carboxylic acid functional group, which can form salt forms with various bases. Overall, (S)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic acid is a versatile compound with potential applications in the field of medicinal chemistry. Its unique chemical structure and biological activities make it an interesting target for drug discovery and development.

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