874974-85-3

Basic information

• Product Name: Benzonitrile, 3-(difluoromethyl)-5-hydroxy-
• CAS NO: 874974-85-3
• Molecular Formula: C8H5F2NO
• Molecular Weight: 169.131
• Mol File: 874974-85-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 3-(difluoromethyl)-5-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 3-(difluoromethyl)-5-hydroxy-(874974-85-3)
• EPA Substance Registry System: Benzonitrile, 3-(difluoromethyl)-5-hydroxy-(874974-85-3)

Safety Data

• Hazardous Substances Data: 874974-85-3(Hazardous Substances Data)

Upstream product

• 1089730-72-2 3-formyl-5-((4-methoxybenzyl)oxy)benzonitrile 
• 1068604-47-6 3-((4-methoxybenzyl)oxy)-5-vinylbenzonitrile 
• 1213790-87-4 3-chloro-5-((4-methoxybenzyl)oxy)benzonitrile 
• 473923-97-6 3-chloro-5-hydroxybenzonitrile 
• 1089730-71-1 3-(difluoromethyl)-5-((4-methoxybenzyl)oxy)benzonitrile 
• 1007572-09-9 3-difluoromethyl-5-methoxy-benzonitrile 

Downstream Products

• 1068603-76-8 3-difluoromethyl-5-(2,3-difluoro-6-nitro-phenoxy)-benzonitrile 
• 910825-41-1 C₁₅H₇BrF₃NO₂ 
• 1338226-04-2 3-(difluoromethyl)-5-({1-[(4-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridin-3-yl}oxy)benzonitrile 
• 874974-86-4 C₁₈H₁₃F₃N₂O₅ 

Relevant articles and documents

PYRIMIDONE DERIVATIVES AS SELECTIVE CYTOTOXIC AGENTS AGAINST HIV INFECTED CELLS

The present disclosure is directed to pyrimidone derivatives of Formula I and their use for selectively killing HIV infected GAG-POL expressing cells without concomitant cytotoxicity to HIV nave cells, and for the treatment or prophylaxis of infection by HIV, or for the treatment, prophylaxis or delay in the onset or progression of AIDS or AIDS Related Complex (ARC).

HETEROCYCLIC ANTIVIRAL COMPOUNDS

The present invention relates to a method of treating an HIV-I infection with a compound according to formula I where R1, R2, R3, R4, R5, are as defined herein.

PROCESS FOR PREPARING TRIAZOLONES

The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones