4681-17-8

Usage

Uses

Used in Cosmetic and Personal Care Industry:
2,3,5-Trichlorobenzyl alcohol is used as a preservative in cosmetic and personal care products to prevent the growth of microorganisms, ensuring the safety and longevity of these products.
Used in Industrial Applications:
Beyond the cosmetic and personal care sector, 2,3,5-Trichlorobenzyl alcohol is also utilized in other industrial applications, where its preservative qualities are beneficial in maintaining the integrity and stability of various products.
Used as a Disinfectant:
2,3,5-Trichlorobenzyl alcohol is employed as a disinfectant due to its ability to kill or inhibit the growth of microorganisms, making it suitable for use in cleaning and sanitizing processes, particularly in environments where hygiene is critical.
Used as an Antiseptic:
In the medical field, 2,3,5-Trichlorobenzyl alcohol serves as an antiseptic, helping to prevent infection by destroying harmful microorganisms on the skin or other surfaces it comes into contact with.

Upstream product

• 56961-75-2 2,3,5-trichlorobenzaldehyde 
• 120-82-1 1,2,4-Trichlorobenzene 
• 50-73-7 2,3,5-trichlorobenzoic acid 

Downstream Products

• 130800-83-8 2,3,5-trichlorophenylmethyl bromide 
• 101084-86-0 2,3,5-trichlorobenzylamine 

Relevant academic research and scientific papers

Systematic Variation of Ligand and Cation Parameters Enables Site-Selective C-C and C-N Cross-Coupling of Multiply Chlorinated Arenes through Substrate-Ligand Electrostatic Interactions

Use of attractive noncovalent interactions between ligand and substrate is an emerging strategy for controlling positional selectivity. A key question relates to whether fine control on molecules with multiple, closely spaced reactive positions is achievable using typically less directional electrostatic interactions. Herein, we apply a 10-piece "toolkit"comprising of two closely related sulfonated phosphine ligands and five bases, each possessing varying cation size, to the challenge of site-selective cross-coupling of multiply chlorinated arenes. The fine tuning provided by these ligand/base combinations is effective for Suzuki-Miyaura coupling and Buchwald-Hartwig coupling on a range of isomeric dichlorinated and trichlorinated arenes, substrates that would produce intractable mixtures when typical ligands are used. This study develops a practical solution for site-selective cross-coupling to generate complex, highly substituted arenes.

Herbicidal 3-(substituted-benzyl)-1-methyl-6-trifluoromethyluracils

Herbicidal 3-(substituted-benzyl)-1-methyl-6-trifluoromethyluracils, compositions containing them, and methods of using them to control undesired plant growth, including use to control weeds in certain crops, are disclosed. The herbicidal compounds of the present invention are defined by the following generic structure: STR1 in which V is hydrogen, halogen, nitro, amino, alkoxy, alkyl, cyano, phenyl, alkylcarbonylamino, alkylsulfinyl, or haloalkyl; W is hydrogen, halogen, alkyl, alkoxy, alkylaminocarbonyl, propargyloxy, cyano, nitro, benzoyl, aminooxycarbonyl, alkylsulfonyl, alkoxyiminoalkyl, alkylthio or alkylsulfinyl; X is hydrogen, chlorine, alkoxy, nitro, or amino; Y is hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkoxyalkyl, alkylthio, alkylthioalkyl, alkenyl, acyl, epoxyalkyl, cyano, alkylaminocarbonyl, carboxy, formyl, hydroxy, hydroxyalkyl, haloalkylsulfonyloxy, benzoyl, aminooxycarbonyl, alkoxycarbonyl, propargyloxy, alkylsulfonyl, alkylsulfinyl, alkoxyiminoalkyl, or dialkylaminocarbonylthio; X and Y taken together are --OCH2 O-- or --OC(CH3)2 O--, where halogen is bromine, chlorine, fluorine, or iodine, and each aliphatic moiety has one to three carbon atoms.

Herbicidal 3-(substituted-benzyl)-1-methyl-6-trifluoromethyluracils

Herbicidal 3-(substituted-benzyl)-1-methyl-6-trifluoromethyluracils, compositions containing them, and methods of using them to control undesired plant growth, including use to control weeds in certain crops, are disclosed. The herbicidal compounds of the present invention are defined by the following generic structure: STR1 in which V is hydrogen or halogen; W is hydrogen, halogen, lower alkoxy, lower alkylaminocarbonyl, propargyloxy, or cyano; X is hydrogen or chlorine; and Y is hydrogen, halogen, cyano, lower alkylaminocarbonyl, or carboxy.

Pharmacologically active CNS compound

The invention provides a series of compounds of formula (I) and salts thereof, wherein for example,R1 and R2, which may be the same or different each represent -NR13R14 where R13 and R14 may each independently represent hydrogen or alkyl or, taken together with the nitrogen atom to which they are attached form a heterocyclic ring, optionally substituted by one or more alkyl or arylalkyl groups and optionally containing a further heteroatom;, R3 is hydrogen, haloalkyl, alkoxymethyl or alkyl;, R4 is hydrogen, nitro or halo;, R5 is hydrogen or halo;, R6 is hydrogen, halo, nitro, amino, alkylamino or dialkylamino;, R7 is hydrogen or halo;, R8 is hydrogen or halo; The compounds may be used for the treatment or prophylaxis of a neurodegenerative or other neurological disorder of the CNS, the aetiology or which includes excessive release of the neurotransmitter glutamate.