35841-84-0

Usage

Usage

Herbicide for controlling weed growth in agricultural crops

Mechanism of action

Inhibits electron transport process in plants, leading to their death

Physical appearance

White crystalline solid

Odor

Slightly musty

Solubility

Sparingly soluble in water

Classification

Potentially harmful substance

Precaution

Should be handled with care to avoid health and environmental risks

InChI:InChI=1/C7H13N5/c1-7(2,3)4-10-5(8)12-6(9)11-4/h1-3H3,(H4,8,9,10,11,12)

Upstream product

• 1070217-24-1 4-tert-butyl-6-chloro-1,3,5-triazin-2-amine 
• 175204-56-5 4-tert-butyl-6-methylsulfanyl-1,3,5-triazin-2-amine 
• 3282-30-2 pivaloyl chloride 
• 705-23-7 2-tert-butyl-4,6-dichloro-[1,3,5]-triazine 

Relevant academic research and scientific papers

HERBICIDAL AZINES

The present invention relates to diaminotriazine compounds of the formula (I) and to their use as herbicides. The present invention also relates to agrochemical compositions for crop protec- tion and to a method for controlling unwanted vegetation, wherein all variable as are defined in claim 1 including their agriculturally acceptable salts.

Catalytic C-Alkylation of Pyrroles with Primary Alcohols: Hans Fischer's Alkali and a New Method with Iridium P,N,P-Pincer Complexes

Hydrogen-autotransfer alkylation (HAT or “borrowing-hydrogen” alkylation) of heteroaromatic compounds has been studied with a range of substrates recently, but pyrroles have been largely absent from such studies. The conditions for HAT alkylations of pyrroles were investigated under a variety of conditions and were found to take place under basic alcoholic conditions (Hans Fischer alkylation) in the absence of transition-metal catalysts; by means of a heterogeneous Pd/C catalyst in the presence of base; and finally by means of homogeneous transition-metal catalysis combining a base and iridium pincer complexes generated in situ that have not previously been used in HAT alkylations of heterocycles.