71422-80-5

Usage

Molecular structure

The compound has a complex molecular structure, consisting of a benzyl group with two trifluoromethyl substituents, a pyridine ring, and a carboxylic acid group.

Functional groups

The compound contains a ketone functional group, indicating that it is a type of organic molecule known as a pyridinecarboxylic acid.

Molecular weight

The molecular weight of the compound is approximately 391.26 g/mol.

Potential applications

The compound may have potential applications in pharmaceuticals, agrochemicals, or other industrial uses, although further research would be needed to fully understand its properties and potential uses.

Stability

The stability of the compound is not mentioned in the material provided, but it is generally expected that the compound would be stable under normal conditions due to the presence of the aromatic ring and the carboxylic acid group.

Solubility

The solubility of the compound is not mentioned in the material provided, but it is likely to be soluble in organic solvents such as ethanol, methanol, or acetone due to the presence of the aromatic ring and the carboxylic acid group.

Reactivity

The reactivity of the compound is not mentioned in the material provided, but it is expected to be reactive with nucleophiles due to the presence of the ketone functional group and the carboxylic acid group.

Synthesis

The synthesis of the compound is not mentioned in the material provided, but it is likely to involve the formation of the benzyl group with the trifluoromethyl substituents, followed by the formation of the pyridine ring and the carboxylic acid group.

Safety

The safety of the compound is not mentioned in the material provided, but it is generally expected that the compound would be handled with care due to the presence of the trifluoromethyl groups, which can be hazardous if inhaled or ingested.

Upstream product

• 69045-84-7 2,3-dichloro-5-trifluoromethylpyridine 
• 91618-22-3 2-(4-nitrophenoxy)-3-chloro-5-trifluoromethyl pyridine 
• 100-02-7 4-nitro-phenol 
• 7439-89-6 iron 

Relevant academic research and scientific papers

Aryloxy anilino propionic ester compound and application thereof as herbicide

An aryloxy anilino propionic ester compound comprises the structure shown in the general formula (I), wherein Ar is aromatic heterocycle or fused heterocycle. Please see the specification for the chemical formula of the aromatic heterocycle and the chemical formula of the fused heterocycle, wherein R1, R2, R3 and R4 are one or more of H, halogen, nitro, methoxy group, methyl, methyl formate group, cyanogroup and trihalomethyl, R5 is the alkyl group on the linear chain or branched chain of H and C1-C4, hydrogen on the alkyl group is substituted by hydroxyl, carboxyl, mercapto group, amino, guanidyl and phenyl, and R6 is one of methyl, ethyl, butyl and the substance specified in the specification. The compound has the advantages that the characteristics of being efficient, capable of acting quickly and not prone to resistance generation of (aryloxy) phenoxypropionate herbicides can be maintained, amino acid functional groups in molecules can be designed to serve as adulterate amino acid so as to restrain the biosynthesis of protein of plants, and all weeds can be controlled.

Herbicidally active phenoxyalkanecarboxylic acid derivatives

A compound of the formula: STR1 wherein Q1 is CH or N; R is H or C1 -C5 alkyl; X is H, halogen, CF3, or NO2 ; Y is H or halogen; Z is --O-- or --NH--; A is STR2 wherein Q2, and Q3 are each CH or N; R1 and R2 are each H, C1 -C5 alkyl, C1 -C5 alkoxy, or C2 -C6 alkxoycarobnyl; R3, R4, and R5 are each H or C1 -C5 alkyl; R6 is H, halogen, or C1 -C5 alkyl; R7, R8, R9, and R10 are each H or C1 -C5 alkyl; R11 is H, C1 -C5 alkyl, C1 -C5 alkoxy, C2 -C6 alkenyl, C6 -C10 aryl, C7 -C15 aryloxyalkyl, or C7 -C15 aralkyl; R12 and R13 are each H or C1 -C5 alkyl; R14 is C1 -C5 alkyl, C2 -C6 alkenyl, C5 -C10 aryl, or C7 -C15 aralkyl; or R13 and R14 taken together form C3 -C4 alkylene, V1 and V2 are each H, halogen, NO2, CN, or CF3 ; V3 is halogen or CF3 ; W1 is --O-- or --NH--; W2 is --(CH2)n -- wherein n is 0 or 1, or CO; X1 is halogen, or a salt thereof, which is effective as a herbicidal agent.

Insecticidally active 2,6-disubstituted benzimidate derivatives

The present invention provides compounds of formula: STR1 wherein X and Y are each independently selected from fluorine, chlorine, methyl or methoxy and one of X and Y may additionally be hydrogen; R is alkoxy of up to 6 carbon atoms, mono- or dialkylamin