Ethyl6-chloroquinoline-3-carboxylate

95%

Reagent Code: #120597
fingerprint
CAS Number 375854-57-2

science Other reagents with same CAS 375854-57-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.67 g/mol
Formula C₁₂H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD14704943
thermostat Physical Properties
Melting Point 108.4-109.1 °C
Boiling Point 341.9±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.286±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Ethyl 6-chloroquinoline-3-carboxylate is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure is particularly valuable in the synthesis of various pharmaceutical agents, where it serves as a building block for the creation of molecules with potential therapeutic properties. This compound is often employed in the research and development of drugs targeting infectious diseases, due to the quinoline moiety's known biological activity. Additionally, it finds application in the study of chemical reactions and mechanisms, aiding in the advancement of synthetic methodologies. Its role in the production of agrochemicals is also notable, contributing to the development of new pesticides and herbicides. Overall, its versatility makes it a significant compound in both academic and industrial chemical research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White 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 ฿17,208.00
inventory 250mg
10-20 days ฿7,083.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl6-chloroquinoline-3-carboxylate
No image available

Ethyl 6-chloroquinoline-3-carboxylate is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure is particularly valuable in the synthesis of various pharmaceutical agents, where it serves as a building block for the creation of molecules with potential therapeutic properties. This compound is often employed in the research and development of drugs targeting infectious diseases, due to the quinoline moiety's known bi

Ethyl 6-chloroquinoline-3-carboxylate is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure is particularly valuable in the synthesis of various pharmaceutical agents, where it serves as a building block for the creation of molecules with potential therapeutic properties. This compound is often employed in the research and development of drugs targeting infectious diseases, due to the quinoline moiety's known biological activity. Additionally, it finds application in the study of chemical reactions and mechanisms, aiding in the advancement of synthetic methodologies. Its role in the production of agrochemicals is also notable, contributing to the development of new pesticides and herbicides. Overall, its versatility makes it a significant compound in both academic and industrial chemical research.

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...