155020-44-3

Basic information

• Product Name: 2-FLUORO-1,3-DIMETHOXY-4-NITROBENZENE
• Synonyms: 2-FLUORO-1,3-DIMETHOXY-4-NITROBENZENE;2-Fluoro-1,3-dimethoxy-4-nitrobenzene 98%;2-Fluoro-1,3-dimethoxy-4-nitrobenzene98%;1,3-Dimethoxy-2-fluoro-4-nitrobenzene, 2-Fluoro-4-nitroresorcinol dimethyl ether;2,4-Dimethoxy-3-fluoronitrobenzene 98%
• CAS NO: 155020-44-3
• Molecular Formula: C₈H₈FNO₄
• Molecular Weight: 201.1518232
• Product Categories: blocks;NitroCompounds
• Mol File: 155020-44-3.mol
• Article Data: 8

Chemical Properties

• Melting Point: 59-61℃
• Boiling Point: 322℃
• Flash Point: 148℃
• Appearance: /
• Density: 1.310
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-FLUORO-1,3-DIMETHOXY-4-NITROBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FLUORO-1,3-DIMETHOXY-4-NITROBENZENE(155020-44-3)
• EPA Substance Registry System: 2-FLUORO-1,3-DIMETHOXY-4-NITROBENZENE(155020-44-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 155020-44-3(Hazardous Substances Data)

Usage

General Description

2-Fluoro-1,3-dimethoxy-4-nitrobenzene is a specialized organic compound that is composed of a benzene ring integrated with substituent groups such as a nitro group (NO2), two methoxy groups (OCH3) and a fluorine atom. The collective presence of these groups contributes to different physical and chemical properties that could be utilized in various chemical reactions and procedures. Like many other nitrobenzenes, this compound is typically a pale yellowish liquid. It must be handled with care due to its nitro group, which can be potentially explosive under certain conditions. Its usage is mainly in research and development, predominantly in settings such as laboratories and industrial chemical plants.

Upstream product

• 67-56-1 methanol 
• 771-69-7 2,3,4-trifluoronitrobenzene 
• 124-41-4 sodium methylate 

Downstream Products

• 1401998-80-8 3-fluoro-2,4-dihydroxybenzaldehyde 
• 502483-90-1 3-fluoro-2,4-dimethoxybenzaldehyde 
• 905752-13-8 2-fluoro-4-iodo-1,3-dimethoxybenzene 
• 1344684-73-6 6-amino-2-fluoro-3-methoxyphenol 
• 1270166-66-9 8-fluoro-4-methylumbelliferyl 2,3,4-tri-O-acetyl-6-O-((18)O)benzoyl-β-D-(6-(18)O)-galactopyranoside 
• 195136-68-6 1,3-dimethoxy-2-fluorobenzene 
• 103068-40-2 2-fluoro resorcinol 
• 195136-66-4 1-amino-3-fluoro-2,4-dimethoxybenzene 

Relevant articles and documents

8-FLUORO-4-ALKYLUMBELLIFERYL ALPHA-D-GLUCOPYRANOSIDE, BIOLOGICAL STERILIZATION INDICATOR INCLUDING THE SAME AND ITS USE IN A METHOD OF DETERMINING EFFICACY OF A STERILIZATION PROCESS

A self-contained biological sterilization indicator comprises: a housing; bacterial spores comprising, and/or capable of producing, an enzyme capable of catalyzing cleavage of an enzyme substrate; and a frangible container containing a composition, wherein the composition comprises the enzyme substrate, wherein if the frangible container is broken the composition will contact the bacterial spores to form a mixture having an initial pH in the range from 6.0 to 9.0. The enzyme substrate comprises a fluorinated 4'-alkylumbelliferyl α-D-glucopyranoside represented by the structural formula (I), wherein R is an alkyl group having from 1 to 12 carbon atoms. A biological sterilization indicator comprising a kit containing isolated components comprising (i) bacterial spores comprising, and/or capable of producing, an enzyme capable of catalyzing cleavage of the enzyme substrate and a method of assessing efficacy of a sterilization process are also disclosed.

1 -HYDROXY-BENZOOXABOROLES AS ANTIPARASITIC AGENTS

Provided are compounds useful for controlling endoparasites both in animals and agriculture. Further provided are methods for controlling endoparasite infestations of an animal by administering an effective amount of a compound as described above, or a pharmaceutically acceptable salt thereof, to an animal, as well as formulations for controlling endoparasite infestations using the compounds described above or an acceptable salt thereof, and an acceptable carrier. The claimed compounds are described by the following Markush formula:A typical example for a compound according to above formula is: A typical example for a compound according to above formula is:

NOVEL TUBULIN POLYMERISATION INHIBITORS

The present invention relates to compounds of general formula (I) as tublin polymerisation inhibitors and methods for preparing such compounds.