7-broMo-4,4-diMethyl-3,4-dihydroquinolin-2(1H)-one

Reagent Code: #77381
fingerprint
CAS Number 185316-44-3

science Other reagents with same CAS 185316-44-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.12 g/mol
Formula C₁₁H₁₂BrNO
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of heterocyclic compounds. Its structure makes it valuable for constructing quinoline derivatives, which are often explored for their potential therapeutic properties, including antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is used in the study of structure-activity relationships to optimize drug candidates. Its bromine substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,190.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
7-broMo-4,4-diMethyl-3,4-dihydroquinolin-2(1H)-one
No image available

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of heterocyclic compounds. Its structure makes it valuable for constructing quinoline derivatives, which are often explored for their potential therapeutic properties, including antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is used in the study of structure-activity r

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of heterocyclic compounds. Its structure makes it valuable for constructing quinoline derivatives, which are often explored for their potential therapeutic properties, including antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is used in the study of structure-activity relationships to optimize drug candidates. Its bromine substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.

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...