(S)-1-BOC-3,4-DIHYDRO-2H-QUINOLINE-2-CARBOXYLIC ACID

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Reagent Code: #37941
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CAS Number 1187933-14-7

science Other reagents with same CAS 1187933-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.32 g/mol
Formula C₁₅H₁₉NO₄
thermostat Physical Properties
Boiling Point 428.8±44.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.222±0.06 g/cm3(Predicted)
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. It plays a crucial role in the preparation of biologically active molecules, including inhibitors and receptor modulators. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and organic synthesis. Additionally, it is utilized in research for creating complex heterocyclic structures, which are essential in drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,159.00
inventory 100mg
10-20 days ฿14,148.00
inventory 1g
10-20 days ฿52,758.00

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(S)-1-BOC-3,4-DIHYDRO-2H-QUINOLINE-2-CARBOXYLIC ACID
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. It plays a crucial role in the preparation of biologically active molecules, including inhibitors and receptor modulators. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and organic synthesis. Additionally, it is utilized in research for creating complex heterocyclic structures, which are essential in drug discovery and medicinal chemis

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. It plays a crucial role in the preparation of biologically active molecules, including inhibitors and receptor modulators. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and organic synthesis. Additionally, it is utilized in research for creating complex heterocyclic structures, which are essential in drug discovery and medicinal chemistry.

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