tert-Butyl (7-bromoquinolin-4-yl)carbamate

95%

Reagent Code: #37122
fingerprint
CAS Number 1416438-99-7

science Other reagents with same CAS 1416438-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.19 g/mol
Formula C₁₄H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD22690544
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis as an intermediate for the preparation of more complex quinoline derivatives. It is particularly valuable in pharmaceutical research, where it aids in the development of compounds with potential therapeutic properties. The bromine atom on the quinoline ring allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its tert-butyl carbamate group provides protection for amines during multi-step synthetic processes, ensuring selective reactions. This compound is also explored in the creation of fluorescent probes and materials for chemical sensing due to the inherent photophysical properties of the quinoline core.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,839.00
tert-Butyl (7-bromoquinolin-4-yl)carbamate
No image available

Used in organic synthesis as an intermediate for the preparation of more complex quinoline derivatives. It is particularly valuable in pharmaceutical research, where it aids in the development of compounds with potential therapeutic properties. The bromine atom on the quinoline ring allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its tert-butyl carbamate group provides protection for amines during multi-step

Used in organic synthesis as an intermediate for the preparation of more complex quinoline derivatives. It is particularly valuable in pharmaceutical research, where it aids in the development of compounds with potential therapeutic properties. The bromine atom on the quinoline ring allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its tert-butyl carbamate group provides protection for amines during multi-step synthetic processes, ensuring selective reactions. This compound is also explored in the creation of fluorescent probes and materials for chemical sensing due to the inherent photophysical properties of the quinoline core.

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...