4-Chloro-3-(Isopropylcarbamoyl)Phenylboronic Acid

≥97%

Reagent Code: #90633
fingerprint
CAS Number 871332-74-0

science Other reagents with same CAS 871332-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.48 g/mol
Formula C₁₀H₁₃BClNO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This chemical is also employed in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Its boronic acid group makes it valuable in bioconjugation and labeling applications, particularly in the field of medicinal chemistry for targeted drug delivery systems. Additionally, it is utilized in research for the development of new materials with potential applications in electronics and optoelectronics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,573.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Chloro-3-(Isopropylcarbamoyl)Phenylboronic Acid
No image available

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This chemical is also employed in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Its boronic acid group makes it valuable in bioconjugation and labeling applica

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This chemical is also employed in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Its boronic acid group makes it valuable in bioconjugation and labeling applications, particularly in the field of medicinal chemistry for targeted drug delivery systems. Additionally, it is utilized in research for the development of new materials with potential applications in electronics and optoelectronics.

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...