(2-Chloro-6-methylquinolin-3-yl)methanol

95%

Reagent Code: #166767
fingerprint
CAS Number 123637-97-8

science Other reagents with same CAS 123637-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.66 g/mol
Formula C₁₁H₁₀ClNO
badge Registry Numbers
MDL Number MFCD02232327
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in the preparation of kinase inhibitors and antimicrobial agents due to the quinoline core's affinity for biological targets. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and selectivity.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28,000.00
inventory 250mg
10-20 days ฿13,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2-Chloro-6-methylquinolin-3-yl)methanol
No image available

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in the preparation of kinase inhibitors and antimicrobial agents due to the quinoline core's affinity for biological targets. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and se

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in the preparation of kinase inhibitors and antimicrobial agents due to the quinoline core's affinity for biological targets. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and selectivity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...