1143571-79-2

Basic information

• Product Name: 2-fluoro-3-methoxybenzaldehyde oxime
• Synonyms: 2-fluoro-3-methoxybenzaldehyde oxime
• CAS NO: 1143571-79-2
• Molecular Weight: 169.155
• Mol File: 1143571-79-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-fluoro-3-methoxybenzaldehyde oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 2-fluoro-3-methoxybenzaldehyde oxime(1143571-79-2)
• EPA Substance Registry System: 2-fluoro-3-methoxybenzaldehyde oxime(1143571-79-2)

Safety Data

• Hazardous Substances Data: 1143571-79-2(Hazardous Substances Data)

Upstream product

• 321-28-8 1-fluoro-2-methoxybenzene 
• 103438-88-6 2-fluoro-3-methoxybenzaldehyde 

Downstream Products

• 1143571-71-4 2-fluoro-3-methoxybenzylamine hydrochloride 
• 198204-64-7 2-fluoro-3-methoxybenzamide 
• 1415718-95-4 C₈H₈FNOS 
• 1415718-97-6 C₁₇H₁₄FNO₂S 
• 1202182-71-5 N-(2-fluoro-3-hexyloxyphenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-69-1 N-(2-fluoro-3-pentyloxyphenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-89-5 N-(3-(3-ethoxypropoxy)-2-fluorophenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-81-7 N-(2-fluoro-3-(4-methoxybutoxy)phenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-87-3 N-(3-(2-ethoxyethoxy)-2-fluorophenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-79-3 N-(2-fluoro-3-(3-methoxypropoxy)phenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-67-9 N-(3-butoxy-2-fluorophenyl)methyl-benzothiazole-6-carboxamide 
• 1202182-85-1 N-(2-fluoro-3-(2-methoxyethoxy)phenyl)methyl-benzothiazole-6-carboxamide 
• 1146493-92-6 2-fluoro-3-hydroxybenzylamine hydrobromide 
• 1202182-65-7 N-(2-fluoro-3-propoxyphenyl)methyl-benzothiazole-6-carboxamide 

Relevant articles and documents

BORON-CONTAINING SMALL MOLECULES

This invention provides novel compounds of the following formula and pharmaceutical compositions containing such compounds.

Optimization of thiazole analogues of resveratrol for induction of NAD(P)H:quinone reductase 1 (QR1)

NAD(P)H:quinone reductase 1 (QR1) belongs to a class of enzymes called cytoprotective enzymes. It exhibits its cancer protective activity mainly by inhibiting the formation of intracellular semiquinone radicals, and by generating α-tocopherolhydroquinone, which acts as a free radical scavenger. It is therefore believed that QR1 inducers can act as cancer chemopreventive agents. Resveratrol (1) is a naturally occurring stilbene derivative that requires a concentration of 21 μM to double QR1 activity (CD = 21 μM). The stilbene double bond of resveratrol was replaced with a thiadiazole ring and the phenols were eliminated to provide a more potent and selective derivative 2 (CD = 2.1 μM). Optimizing the substitution pattern of the two phenyl rings and the central heterocyclic linker led to a highly potent and selective QR1 inducer 9o with a CD value of 0.087 μM.

N-BENZYL QUINOLINE-6-CARBOXAMIDE COMPOUNDS AND PLANT DISEASE CONTROLLING METHOD USING SAME

The object of the present invention is to provide a compound having excellent controlling effect on plant diseases. An amide compound represented by the following formula (I) has excellent controlling effect on plant diseases: (in the formula, R denotes a