2-AMINO-3-(1,2-DIHYDRO-2-OXOQUINOLINE-4-YL)PROPANOIC ACID HYDROCHLORIDE

≥99.5%

Reagent Code: #73321
label
Alias Related CAS: 5162-90-3
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CAS Number 132210-24-3

science Other reagents with same CAS 132210-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.7?anhy? g/mol
Formula C₁₂H₁₃ClN₂O₃
badge Registry Numbers
EC Number 1312995-182-4
thermostat Physical Properties
Melting Point 220-221 ºC
Boiling Point 522.716 ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.344 g/cm3
Storage room temperature

description Product Description

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a quinoline core, makes it a valuable intermediate in the design of molecules targeting various biological pathways. It is often explored for its potential in creating compounds with anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its amino acid moiety allows for integration into peptide-based therapeutics, enhancing binding affinity and specificity. Researchers also utilize it in studying enzyme inhibition and receptor modulation due to its unique chemical framework.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,368.00
inventory 25g
10-20 days ฿3,852.00
inventory 100g
10-20 days ฿11,520.00
inventory 500g
10-20 days ฿32,220.00

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2-AMINO-3-(1,2-DIHYDRO-2-OXOQUINOLINE-4-YL)PROPANOIC ACID HYDROCHLORIDE
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This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a quinoline core, makes it a valuable intermediate in the design of molecules targeting various biological pathways. It is often explored for its potential in creating compounds with anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its amino acid moiety allows for integration into peptide-based therapeutics, enhancing binding

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a quinoline core, makes it a valuable intermediate in the design of molecules targeting various biological pathways. It is often explored for its potential in creating compounds with anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its amino acid moiety allows for integration into peptide-based therapeutics, enhancing binding affinity and specificity. Researchers also utilize it in studying enzyme inhibition and receptor modulation due to its unique chemical framework.

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