98280-32-1

Usage

Uses

Used in Chemical Synthesis:
(4-CHLORO-6-METHYL-PYRIDIN-2-YL)-METHANOL is used as a reagent in chemical synthesis for its reactivity, contributing to the formation of various compounds and products.
Used in Research and Development:
(4-CHLORO-6-METHYL-PYRIDIN-2-YL)-METHANOL is used as a research compound for exploring its potential applications in different industries, as its properties and reactivity are still being studied and understood.
Used in Industrial Applications:
(4-CHLORO-6-METHYL-PYRIDIN-2-YL)-METHANOL is used as a chemical intermediate in various industrial processes, where its unique structure and reactivity can be leveraged to produce desired outcomes.

Upstream product

• 315494-03-2 ethyl 4-chloro-6-methylpyridine-2-carboxylate 
• 339585-99-8 acetic 4-chloro-6-methyl-2-pyridinylmethyl ester 
• 697-92-7 2,6-dimethyl-4-chloropyridine N-oxide 

Downstream Products

• 98273-77-9 4-chloro-6-methylpicolinaldehyde 

Relevant academic research and scientific papers

Oxime O-ether compounds and fungicides for agricultural and horticultural use

The present invention relates to novel oxime O-ether compounds represented by a general formula [I]; wherein R1represents C1-6alkyl, C3-6cycloalkyl, C1-6alkoxy, etc., m represents an integer of 1 to 4, R2/

OXIME ETHER COMPOUND AND AGRICULTURAL OR HORTICULTURAL BACTERICIDE

An oxime ether compound represented by the formula [I] or a salt thereof which have excellent bactericidal activity and are useful as an agricultural or horticultural fungicide. [I] (In the formula, R1 represents halogeno, hydroxy, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkyl substituted by C1-6 alkoxy, cyano, nitro, C2-6 alkenyl, C2-6 haloalkenyl, C2-6 alkynyl, amino, mono(C1-6 alkyl)amino, di(C1-6 alkyl)amino, C3-6 cycloalkyl, carboxyl, C1-6 alkoxycarbonyl, etc.; R2 represents hydrogen, C1-6 alkyl, C3-6 cycloalkyl, C1-6 haloalkyl, etc.; R3 and R4 each represents hydrogen or C1-6 alkyl; k is an integer of 1 to 4; and A represents the heterocyclic group shown in the description.)

ACYLHYDRAZINE DERIVATIVES, PROCESS FOR PREPARING THE SAME AND USE THEREOF

Novel acylhydrazine derivatives exhibiting an inhibitory activity against activated blood coagulation factor X, which are compounds of general formula (I)or salts thereof, wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; R1and R2are each hydrogen or optionally substituted hydrocarbyl, or alternatively R1and R2or the substituent of X1and R2may be united to form an optionally substituted ring; X1and X2are each free valency, optionally substituted alkylene, or optionally substituted imino; D is oxygen or sulfur; A is -N(R3)-Y- or -N=Y-, R3is hydrogen, optionally substituted hydrocarbyl, or acyl; Y is an optionally substituted chain hydrocarbon group or an optionally substituted cyclic group; and Z is (1) optionally substituted amino, (2) optionally substituted imidoyl, or (3) an optionally substituted nitrogenous heterocycle group.