(3-Chloro-4-(2-(4-ethylpiperazin-1-yl)ethoxy)phenyl)boronic acid

98%

Reagent Code: #90198
fingerprint
CAS Number 1704074-31-6

science Other reagents with same CAS 1704074-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.61 g/mol
Formula C₁₄H₂₂BClN₂O₃
badge Registry Numbers
MDL Number MFCD28400368
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of new drugs. Its boronic acid group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds. This is essential in creating complex organic molecules, including potential therapeutic agents.

In medicinal chemistry, it serves as a building block for designing molecules that target specific biological pathways. Its structure, featuring a piperazine moiety, is often incorporated into compounds intended for central nervous system (CNS) drug development, as piperazine derivatives are known for their ability to interact with neurotransmitter receptors.

Additionally, its chloro and ethoxy substituents enhance its reactivity and selectivity, making it useful in synthesizing compounds with potential anticancer, antiviral, or antibacterial properties. Researchers also explore its role in developing inhibitors for enzymes or proteins involved in disease processes. Overall, it is a versatile intermediate in drug discovery and chemical synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿36,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-Chloro-4-(2-(4-ethylpiperazin-1-yl)ethoxy)phenyl)boronic acid
No image available

This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of new drugs. Its boronic acid group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds. This is essential in creating complex organic molecules, including potential therapeutic agents.

In medicinal chemistry, it serves as a building block for designing molecules that target specific biological pathways. Its stru

This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of new drugs. Its boronic acid group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds. This is essential in creating complex organic molecules, including potential therapeutic agents.

In medicinal chemistry, it serves as a building block for designing molecules that target specific biological pathways. Its structure, featuring a piperazine moiety, is often incorporated into compounds intended for central nervous system (CNS) drug development, as piperazine derivatives are known for their ability to interact with neurotransmitter receptors.

Additionally, its chloro and ethoxy substituents enhance its reactivity and selectivity, making it useful in synthesizing compounds with potential anticancer, antiviral, or antibacterial properties. Researchers also explore its role in developing inhibitors for enzymes or proteins involved in disease processes. Overall, it is a versatile intermediate in drug discovery and chemical synthesis.

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...