4-QUinolinecarboxamide, N-[3-[[[2-[4-(aminosulfonyl)phenyl]ethyl]amino]carbonyl]phenyl]-1,2-dihydro-2-oxo-

98%

Reagent Code: #228500
fingerprint
CAS Number 939760-13-1

science Other reagents with same CAS 939760-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.53 g/mol
Formula C₂₅H₂₂N₄O₅S
badge Registry Numbers
MDL Number MFCD09282757
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of sulfa drugs, particularly in the development of sulfonamide-based antibiotics. It plays a role in creating compounds with antimicrobial properties by serving as a building block in medicinal chemistry. Its structure supports the inhibition of bacterial folic acid synthesis, making it valuable in designing agents active against a range of pathogens. Also investigated for use in anti-inflammatory and anticancer research due to its ability to modify enzyme activity in targeted therapies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿8,000.00
inventory 50mg
10-20 days ฿30,380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-QUinolinecarboxamide, N-[3-[[[2-[4-(aminosulfonyl)phenyl]ethyl]amino]carbonyl]phenyl]-1,2-dihydro-2-oxo-
No image available

Used as an intermediate in the synthesis of sulfa drugs, particularly in the development of sulfonamide-based antibiotics. It plays a role in creating compounds with antimicrobial properties by serving as a building block in medicinal chemistry. Its structure supports the inhibition of bacterial folic acid synthesis, making it valuable in designing agents active against a range of pathogens. Also investigated for use in anti-inflammatory and anticancer research due to its ability to modify enzyme activit

Used as an intermediate in the synthesis of sulfa drugs, particularly in the development of sulfonamide-based antibiotics. It plays a role in creating compounds with antimicrobial properties by serving as a building block in medicinal chemistry. Its structure supports the inhibition of bacterial folic acid synthesis, making it valuable in designing agents active against a range of pathogens. Also investigated for use in anti-inflammatory and anticancer research due to its ability to modify enzyme activity in targeted therapies.

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...