(S)-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLIC ACID

≥95%

Reagent Code: #37850
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CAS Number 92976-98-2

science Other reagents with same CAS 92976-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.2 g/mol
Formula C₁₀H₁₁NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

(S)-1,2,3,4-Tetrahydro-quinoline-2-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure serves as a building block for developing drugs with potential therapeutic effects, particularly in the treatment of neurological disorders and cardiovascular diseases. The compound is also explored in the design of enzyme inhibitors, targeting specific biological pathways to modulate disease progression. Additionally, it finds application in research settings for studying chiral molecules and their interactions, aiding in the development of enantioselective synthesis methods. Its versatility makes it a valuable component in drug discovery and organic synthesis.

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inventory 1g
10-20 days ฿9,828.00

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(S)-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLIC ACID
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(S)-1,2,3,4-Tetrahydro-quinoline-2-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure serves as a building block for developing drugs with potential therapeutic effects, particularly in the treatment of neurological disorders and cardiovascular diseases. The compound is also explored in the design of enzyme inhibitors, targeting specific biological pathways to modulate disease progression. Add

(S)-1,2,3,4-Tetrahydro-quinoline-2-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure serves as a building block for developing drugs with potential therapeutic effects, particularly in the treatment of neurological disorders and cardiovascular diseases. The compound is also explored in the design of enzyme inhibitors, targeting specific biological pathways to modulate disease progression. Additionally, it finds application in research settings for studying chiral molecules and their interactions, aiding in the development of enantioselective synthesis methods. Its versatility makes it a valuable component in drug discovery and organic synthesis.

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