(4-Bromo-5-chlorothiophen-2-yl)boronic acid

96%

Reagent Code: #119356
fingerprint
CAS Number 1150114-72-9

science Other reagents with same CAS 1150114-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.3 g/mol
Formula C₄H₃BBrClO₂S
badge Registry Numbers
MDL Number MFCD12025986
inventory_2 Storage & Handling
Storage -20°C, dark, inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their biological activities, making it valuable in drug discovery and development. Additionally, it can be utilized in material science for creating advanced polymers or electronic materials with specific properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-Bromo-5-chlorothiophen-2-yl)boronic acid
No image available

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their biological activities, making it valuable in drug discovery and devel

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their biological activities, making it valuable in drug discovery and development. Additionally, it can be utilized in material science for creating advanced polymers or electronic materials with specific properties.

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...