3065-27-8

Usage

Uses

Used in Pesticide Applications:
2,4,5-trichlorophenyl 3-phenyl-N-[(phenylmethoxy)carbonyl]-L-alaninate is used as a pesticide or herbicide for its ability to inhibit the growth of unwanted plants or pests. It works by interfering with vital metabolic processes in the target organisms, ultimately leading to their death. This makes it an effective tool in controlling unwanted vegetation and pests in agricultural settings.
Used in Chemical Synthesis:
2,4,5-trichlorophenyl 3-phenyl-N-[(phenylmethoxy)carbonyl]-L-alaninate can also be used as an intermediate in the synthesis of other chemical compounds. Its unique structure and reactivity make it a valuable component in the creation of various chemical products, contributing to the development of new materials and substances.
Used in Agricultural Industry:
In the agricultural industry, 2,4,5-trichlorophenyl 3-phenyl-N-[(phenylmethoxy)carbonyl]-L-alaninate is used as a herbicide to control the growth of weeds and other unwanted plants. This helps to improve crop yield and quality by reducing competition for resources such as nutrients, water, and sunlight.
Used in Pest Control Industry:
In the pest control industry, 2,4,5-trichlorophenyl 3-phenyl-N-[(phenylmethoxy)carbonyl]-L-alaninate is used as a pesticide to manage and eliminate pests that can cause damage to crops and stored products. Its effectiveness in disrupting the metabolic processes of pests makes it a reliable option for integrated pest management strategies.

InChI:InChI=1/C23H18Cl3NO4/c24-17-12-19(26)21(13-18(17)25)31-22(28)20(11-15-7-3-1-4-8-15)27-23(29)30-14-16-9-5-2-6-10-16/h1-10,12-13,20H,11,14H2,(H,27,29)

Upstream product

• 1161-13-3 N-Cbz-L-Phe 
• 95-95-4 2,4,5-trichlorophenol 
• 16947-69-6 2,4,5-Trichlorophenyl chloroformate 
• 13795-27-2 (2,4,5-Trichlorphenyl)-benzyl-carbonat 
• 16480-57-2 L-phenylalanine sodium salt 

Downstream Products

• 69193-13-1 Cbz-L-Phe-L-Leu-NH₂ 
• 71450-10-7 benzyl N-((1S)-2-[(1S)-1-(aminocarbonyl)-3-(methylsulfanyl)propyl]amino-1-benzyl-2-oxoethyl)carbamate 
• 91291-34-8 Z-Phe-Val-Sta-Ala-Sta-OCH₃ 
• 92628-14-3 Z-Phe-Ile-Sta-Ala-Sta-OCH₃ 
• 92608-46-3 Z-Phe-Pro-Sta-Ala-Sta-OCH₃ 
• 91291-37-1 Z-Phe-D-Phe-Sta-Ala-Sta-OCH₃ 
• 91291-37-1 Z-Phe-Phe-Sta-Ala-Sta-OCH₃ 
• 91291-43-9 Z-Phe-Trp-Sta-Ala-Sta-OCH₃ 
• 16947-10-7 N--funtumin 
• 16947-14-1 3β-<(Benzyloxycarbonyl-Phe-Gly)-amino>-5β-pregnanon-(20) 

Relevant academic research and scientific papers

A remarkable catalytic effect of the potassium salt of 1-hydroxybenzotriazole on peptide bond formation

A semiquantitative investigation was done on the catalytic effects of 1-hydroxybenzotriazole (HOBt) (5) and the potassium salt 6 of HOBt (5) on peptide bond formation by the active ester method. HOBt (5) was found to catalyze the aminolysis reaction of two different types of active esters, benzyloxy-carbonyl-l-phenylalanine 2,4,5-trichlorophenyl ester (1) and benzyloxycarbonyl-l-phenylalanine 1-succinimidyl ester (2), in tetrahydrofuran (THF) and in a dipolar aprotic dimethylformamide (DMF) solvent. A large rate enhancement was also observed in the aminolysis reaction of 1 in THF when the potassium salt 6 of HOBt (5) was added in the presence of dicyclohexyl-18-crown-6 (7). The rate acceleration in the aminolysis reaction of the active esters by 5 and 6 may reasonably be explained in terms of nucleophilic catalysis.

Novel esterifying agents, and their production and use

A process for esterifying organic carboxylic acids which comprises reacting an organic carboxylic acid with a carbonic acid ester of the formula: EQU1 wherein R is an organic group and X and Y are each a negative group in the presence of a basic substance to make esterified the carboxyl group in the organic carboxylic acid. The process is advantageous in affording the objective carboxylic ester in a good yield within a short time by a simple operation under a mild reaction condition.