185950-64-5

Basic information

• Product Name: (5-Chloro-2-pivalaMidophenyl)boronic acid
• Synonyms: (5-Chloro-2-pivalaMidophenyl)boronic acid;5-Chloro-2-(pivaloylamino)phenylboronic acid
• CAS NO: 185950-64-5
• Molecular Formula: C₁₁H₁₅BClNO₃
• Molecular Weight: 255.5057
• Mol File: 185950-64-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (5-Chloro-2-pivalaMidophenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (5-Chloro-2-pivalaMidophenyl)boronic acid(185950-64-5)
• EPA Substance Registry System: (5-Chloro-2-pivalaMidophenyl)boronic acid(185950-64-5)

Safety Data

• Hazardous Substances Data: 185950-64-5(Hazardous Substances Data)

Usage

General Description

(5-Chloro-2-pivalamidophenyl)boronic acid is a chemical compound with the formula C12H16BClNO2. It is commonly used as a building block in organic synthesis and pharmaceutical research. (5-Chloro-2-pivalaMidophenyl)boronic acid has been explored for its potential use in the development of medicinal products, particularly in the field of cancer research. It is also used as a reagent in the Suzuki-Miyaura cross-coupling reaction, allowing for the creation of complex organic molecules. Additionally, it has been studied for its potential application in the treatment of various diseases due to its ability to target specific biological pathways and proteins. Overall, (5-Chloro-2-pivalamidophenyl)boronic acid is a versatile chemical with potential applications in various fields of research and development.

Upstream product

• 121-43-7 Trimethyl borate 
• 65854-91-3 N-(4-chlorophenyl)-2,2-dimethylpropionamide 

Downstream Products

• 359844-90-9 2-[(2H)-2-methyl-3-oxo-5-pyridazinyl]-4-chloro-N-pivaloylanilide 
• 874955-82-5 4-(5-chloro-2-pivaloylaminophenyl)-2-methyl-6-nitropyridazin-3(2H)-one 
• 870556-04-0 4-chloro-2-pyridin-2-yl-phenylamine 
• 1346156-11-3 9-chloro-3-methyl-5-phenylamino-pyridazino[4,5-c]quinolin-4(3H)-one 
• 1346156-14-6 5-[2-(1,6-dihydro-1-methyl-6-oxopyridazin-4-yl)-4-chlorophenyl-amino]-9-chloro-3-methyl-pyridazino[4,5-c]quinolin-4(3H)-one 
• 1346156-08-8 5-(5-chloro-2-triphenylphosphoranylideneaminophenyl)-2-methylpyridazin-3(2H)-one 
• 359844-94-3 5-(2-azido-5-chlorophenyl)-2-methylpyridazin-3(2H)-one 
• 359844-92-1 5-(2-amino-5-chlorophenyl)-2-methylpyridazin-3(2H)-one 
• 518051-01-9 6-(2-amino-5-chlorophenyl)-1,3-dimethyluracil 
• 518050-99-2 N-[4-chloro-2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl]pivalamide 

Relevant articles and documents

CCR2 INHIBITORS AND METHODS OF USE THEREOF

Compounds are provided that act as potent antagonists of the CCR2 or CCR9 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR2 and CCR9. The compounds are generally aryl sulfonamide d