66346-05-2

Usage

General Description

1H-1,2,4-Triazole-1-ethanol, b-[(4-chlorophenyl)methyl]-a-(1,1-dimethylethyl)-, (aS,bS)-, also known as Terconazole, is a potent antifungal medication used to treat vaginal yeast infections. It works by interfering with the synthesis of the cell membrane of the fungus, leading to its death. Terconazole is available in various forms, such as vaginal suppositories and creams, and is typically applied once daily for a prescribed period of time. This medication is generally well-tolerated but may cause mild side effects such as irritation and burning at the application site. It is important to follow the dosage instructions provided by a healthcare professional to ensure the safe and effective use of Terconazole.

Upstream product

• 63190-87-4 1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-one 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 5469-26-1 1-Bromopinacolon 
• 58905-32-1 3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanone 
• 66346-01-8 1-(4-chlorophenyl)-4,4-dimethyl-pentan-3-one 
• 109-65-9 1-bromo-butane 
• 693-03-8 n-butyl magnesium bromide 
• 66346-00-7 α-(1,2,4-triazol-1-yl)-α-p-chlorobenzylchloride 
• 124339-88-4 1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-one 
• 124339-89-5 1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-one 

Relevant academic research and scientific papers

Plant growth regulating formulations

Plant growth regulating preparations comprising: (a) 0.1-20 wt. % of a 16,17-dihydro gibberellin of formula (Ia) or (Ib); (b) up to 99.9 wt. % of a formulation additive selected from: (b1) the reaction products of triglycerides based on carboxylic acids having 2-30C and ethylene oxide and/or propylene oxide in the presence of a base, and/or (b2) fatty acid alcohol polyethoxylates; (c) up to 50 wt. % of an organic solvent; (d) 0.1-50 wt. % of a formulation auxiliary different from (b1) and (b2); (e) up to 50 wt. % of additional plant growth regulating compounds can be used in agriculture and horticulture to induce the desired effects on, for example, seed germination and seedling growth, rooting, dormancy, juvenility, maturity and senescence, flowering, abscission of leaves, flowers and fruit, fruit set and development, tuber formation, growth of shoot and root, photoassimilation, control of unwanted plants and senescence of whole plants or single organs. The 16,17-dihydroGA's are used to synergize the biological activity of exogenously supplied gibberellins. Particularly in graminaceous species, the compounds synergize the action of exogenous GA's and can, thus, be used to increase the yield of malt and decrease the amount of time required for the malting process, increase the yield of sugar cane and stimulate germination and seedling development in rice, wheat, barley, oats, rye, maize, sorghum, turf grasses and other plant species.

New lead compounds for brassinosteroid biosynthesis inhibitors

The first brassinosteroid biosynthesis inhibitor is reported. Among newly synthesized triazole derivatives, 4-(4-chlorophenyl)-2-phenyl-3- (1,2,4-triazoyl)butan-2-ol (6) was found to inhibit the growth of cress seedlings, and this inhibition was recovered by the treatment of brassinolide, suggesting that compound 6 primarily inhibits brassinosteroid biosynthesis.

Patch preparations for treating plants

The following invention introduces a patch preparation for treating plants, whereas the patch preparations comprise a chemical layer composed of at least one agrochemically active compound, at least one adhesive and optionally, one or more additives. The components are dispersed in a matrix state on a substrate which are then introduced on the roots of the plant to be treated.

Method for the treatment of plants with agrochemical tablet compositions

Novel method for applying agrochemicals to plants, which method consists in attaching to the surface of the plants tablets comprising at least one agrochemically active compound and at least one adjuvant, which is solid, liquid of pasty at room temperature, and optionally, one or more excipients optionally in admixture with one or more other additives and/or water.

Use of diphenyl ether derivatives for the desiccation and abscission of plant organs

The use of diphenyl ether derivatives of the general formula I STR1 where A is a radical STR2 where R1 is hydrogen, an alkali metal or alkaline earth metal ion, substituted or unsubstituted ammonium, alkyl of from 1 to 4 carbon atoms or alkoxycarbonylalkyl of a total of 1 to 6 carbon atoms and R2 is alkyl of from 1 to 4 carbon atoms, for the desiccation and abscission of plant organs.

THE PREPARATION OF ENANTIOMERS OF PACLOBUTRAZOL : A CRYSTAL CHEMISTRY APPROACH

A practical method for preparing the desired enantiomer of an agrochemical is described.The unwanted enantiomer is recycled simultaneously.Development of the method necessitated an understanding of the organic, solution and crystal chemistry.The general a

Combating fungi with triazolyl-benzyloxy-ketones and-carbinols

Triazolyl-benzyloxy-ketones or carbinols of the formula STR1 in which A is a keto group or a CH(OH) group, X is a halogen atom or an alkyl or halogenoalkyl radical, and n is 0, 1, 2, 3, 4 or 5, or an addition product thereof with a physiologically acceptable acid or metal salt, which possess fungicidal properties. Intermediates wherein A is a keto group and the azole group is replaced by chloride or bromine are also new.

Fungicidal compounds

Triazoles of formula: STR1 wherein R1 is alkenyl, alkynyl or optionally substituted aralkyl; Y is =N--, R2 is cycloalkyl, alkyl or haloalkyl, and R3 is H, methyl or alkenyl, or esters, ethers, salts and metal complexes thereof. The triazoles have fungicidal and plant growth regulating activity.