55807-46-0

Usage

InChI:InChI=1/C9H15N3O2/c1-9(2,3)6-5-7(12-14-6)11-8(13)10-4/h5H,1-4H3,(H2,10,11,12,13)

Upstream product

• 81479-48-3 phenyl (5-(tert-butyl)isoxazol-3-yl)carbamate 
• 74-89-5 methylamine 
• 55809-36-4 3-amino-5-tert-butylisoxazole 
• 624-83-9 methyl isocyanate 

Downstream Products

• 55809-36-4 3-amino-5-tert-butylisoxazole 

Relevant academic research and scientific papers

HERBICIDAL MIXTURES

The present invention provides a composition comprising (A) a compound of formula (I): wherein R1 is methyl or methoxy, R2 is hydrogen, methyl or ethoxy and A is a substituted heteroaryl group, or an N-oxide or salt form thereof, and

HERBICIDAL COMPOUNDS

The invention relates to dihydro-hydantoincompounds of the formula (I) wherein X, Rb, Rc, R2 and R3 are as defined in the specification. Furthermore, the present invention relates to processes and intermediates

Isoxazolotriazindiones and plant growth inhibiting use thereof

Certain isoxazolotriazinediones, useful for controlling the growth of unwanted plants.

Herbicidal method for fallow land

A method for controlling unwanted vegetation in fallow land, particularly in fallow wheatland, employing a 3-isoxazolylurea herbicide is described.

3-[5- or 3-Substituted-5- or 3-isoxazolyl]-1-allyl or alkyl-4-substituted-5-substituted or unsubstituted-2-imidazolidinones

Disclosed are compounds such as 3-[5-(1,1-dimethylethyl)-3-isoxazolyl]-1-methyl-4-hydroxy-2-imidazolidinone; their control of weeds such as johnsongrass; the process of making them; and intermediates for making them, the compounds being represented by a Formula I: STR1 wherein A is STR2 where R is an alkyl of up to six carbon atoms; an alkenyl of up to five carbon atoms; an alkynyl of up to five carbon atoms; a cycloalkyl selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl; a haloalkyl of up to six carbon atoms; --R4 --O--R5, or --R4 --S--R5, where R4 is an alkylene of up to six carbon atoms and R5 is an alkyl of up to six carbon atoms; STR3 where Z is nitro (NO2), chloro (Cl), bromo (Br), fluoro (F), or R5, and n is 0, 1, 2, or 3; R1 is an alkyl of up to three carbon atoms, or allyl; R2 is hydroxy (OH), chloro (Cl) or bromo (Br); and R3 is hydrogen (H), an alkyl of up to four carbon atoms, allyl, or hydroxy (OH).

Process for preparing 3-isoxazolylurea derivatives

3-Isoxazolylurea derivatives of the formula: STR1 (wherein R represents hydrogen, C1 -C6 alkyl, or C6 -C8 aryl; R1 represents hydrogen or C1 -C6 alkyl; R2 represents C