103977-78-2

Basic information

• Product Name: 3-Bromo-2,4-difluoronitrobenzene 98%
• Synonyms: 3-Bromo-2,4-difluoronitrobenzene 98%;3-Bromo-2,4-difluoronitrobenzene98%
• CAS NO: 103977-78-2
• Molecular Formula: C₆H₂BrF₂NO₂
• Molecular Weight: 238
• Mol File: 103977-78-2.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 254.0±35.0 °C(Predicted)
• Appearance: /
• Density: 1.890±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Bromo-2,4-difluoronitrobenzene 98%(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-2,4-difluoronitrobenzene 98%(103977-78-2)
• EPA Substance Registry System: 3-Bromo-2,4-difluoronitrobenzene 98%(103977-78-2)

Safety Data

• Hazardous Substances Data: 103977-78-2(Hazardous Substances Data)

Usage

General Description

3-Bromo-2,4-difluoronitrobenzene 98% is a chemical compound with high purity (98%), meaning only 2% of it contains impurities or other substances. 3-Bromo-2,4-difluoronitrobenzene 98%, as the name suggests, has a bromine atom, two fluorine atoms, and a nitro group attached to a benzene ring. It can be used as a starting material or building block in various organic and organometallic reactions, particularly in the synthesis of more complex molecules for use in carry-out research, chemical products production, or drug discovery. The precise roles and reactivity of this compound can vary widely depending on the specific reaction conditions and other reactants present. It should be handled with care due to potential safety hazards associated with many chemical substances and is expected to be stored under specific conditions to maintain its stability and reactivity.

Upstream product

• 64248-56-2 1-bromo-2,6-difluorobenzene 

Downstream Products

• 103977-79-3 2-bromo-1,3-difluoro-4-aminobenzene 
• 103979-08-4 2-bromo-3-fluoro-6-nitrophenol 
• 1257535-06-0 3-bromo-4-fluorobenzene-1,2-diamine 
• 103979-09-5 1-(2-bromo-3-fluoro-6-nitrophenoxy)acetone 

Relevant articles and documents

Structure Based Design of N-(3-((1H-Pyrazolo[3,4-b]pyridin-5-yl)ethynyl)benzenesulfonamides as Selective Leucine-Zipper and Sterile-α Motif Kinase (ZAK) Inhibitors

A series of N-(3-((1H-pyrazolo[3,4-b]pyridin-5-yl)ethynyl)benzenesulfonamides were designed as the first class of highly selective ZAK inhibitors. The representative compound 3h strongly inhibits the kinase activity of ZAK with an IC50 of 3.3 n

GCN2 MODULATOR COMPOUNDS

The disclosures herein relate to novel compounds of Formula (1): or a salt thereof, wherein X, Y, R1, R2, R3, R4 and R5 are defined herein, and their use in treating, preventing, ameliorating, controlling or reducing the risk of disorders associated with General Control Nondepressible 2 (GCN2).

Alkylene phenylsulfonamide type selective ZAK inhibitor and application thereof

The invention relates to application of an alkylene phenylsulfonamide compound with a structure of formula (I) (shown in the description) or pharmaceutically acceptable salt thereof or stereisomer thereof or a prodrug molecule thereof in preparation of a