59843-36-6

Basic information

• Product Name: 1H-Pyrazole, 4-chloro-3-phenyl-
• CAS NO: 59843-36-6
• Molecular Formula: C9H7ClN2
• Molecular Weight: 178.621
• Mol File: 59843-36-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Pyrazole, 4-chloro-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole, 4-chloro-3-phenyl-(59843-36-6)
• EPA Substance Registry System: 1H-Pyrazole, 4-chloro-3-phenyl-(59843-36-6)

Safety Data

• Hazardous Substances Data: 59843-36-6(Hazardous Substances Data)

Upstream product

• 2458-26-6 3-phenylpyrazole 

Downstream Products

• 59843-37-7 2-(4-chloro-3-phenyl-pyrazol-1-yl)-N,N-dimethyl-propionamide 
• 59843-38-8 2-(4-chloro-5-phenyl-pyrazol-1-yl)-N,N-dimethyl-propionamide 
• 59843-81-1 4-chloro-N,N-diethyl-α-methyl-3-phenylpyrazole-1-acetamide 
• 59843-82-2 2-(4-chloro-5-phenyl-pyrazol-1-yl)-N,N-diethyl-propionamide 

Relevant articles and documents

Oxidative Photochlorination of Electron-Rich Arenes via in situ Bromination

Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromide ions, visible light, and 4CzIPN as organic photoredox catalyst. The substrates are brominated in situ in a first photoredox-catalyzed oxidation step, followed by a photocatalyzed ipso-chlorination, yielding the target compounds in high ortho/para regioselectivity. Dioxygen serves as a green and convenient terminal oxidant. The use of aqueous hydrochloric acid as the chloride source reduces the amount of saline by-products.

CARBOXAMIDE COMPOUNDS AND THEIR USE AS CALPAIN INHIBITORS V

The present invention relates to novel carboxamide compounds and their use for the manufacture of a medicament. The carboxamide compounds are inhibitors of calpain (calcium dependant cysteine proteases). The invention therefore also relates to the use of