683223-04-3

Basic information

• Product Name: Urea, N-(2,2-dimethoxyethyl)-N-methyl- (9CI)
• Synonyms: Urea, N-(2,2-dimethoxyethyl)-N-methyl- (9CI);1-(2,2-Dimethoxy-ethyl)-1-methyl-urea
• CAS NO: 683223-04-3
• Molecular Formula: C6H14N2O3
• Molecular Weight: 162.18696
• Product Categories: AMINETERTIARY
• Mol File: 683223-04-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Urea, N-(2,2-dimethoxyethyl)-N-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Urea, N-(2,2-dimethoxyethyl)-N-methyl- (9CI)(683223-04-3)
• EPA Substance Registry System: Urea, N-(2,2-dimethoxyethyl)-N-methyl- (9CI)(683223-04-3)

Safety Data

• Hazardous Substances Data: 683223-04-3(Hazardous Substances Data)

Upstream product

• 624-83-9 methyl isocyanate 
• 22483-09-6 2,2-dimethoxyethylamine 
• 1118-02-1 trimethylsilyl isocyanate 
• 122-07-6 N-(methyl)aminoacetaldehyde dimethyl acetal 

Relevant articles and documents

HERBICIDAL COMPOUNDS

The invention relates to pyrrolone compounds of the formula (I) wherein X, R1, R2, R3, Ra, Rc and Rd are as defined in the specification. Furthermore, the present invention relates to processes and intermediates for making compounds of formula (I), to herbicidal compositions comprising these compounds and to methods of using these compounds to control plant growth.

Imidazolin-2-ones

A compound having the formula: STR1 wherein R, R1 and R2 are independently selected from hydrogen; hydroxy; fluorine; bromine; chlorine; C1 -C20 alkyl; C2 -C20 alkenyl; C2 -C20 alkynyl; C3 -C10 cycloalkyl; C2 -C20 (monohydroxy or polyhydroxy)alkyl; C1 -C20 (monohalo or polyhalo)alkyl; carboxy; C1 -C20 alkylcarboxy; C1 -C20 alkenylcarboxy; C1 -C20 carboxyalkyl; C1 -C20 alkanoyl; C1 -C20 alkanoyloxy; C1 -C20 alkoxycarbonyl; carbamoyl; carbamyl; C1 -C20 alkylcarbamyl; sulfo; C1 -C20 alkylsulfonyl; C1 -C20 alkylsulfinyl; C1 -C20 alkylsulfoxide; C1 -C20 alkylsulfone; thio; C1 -C20 alkylthio; amino; nitro; C1 -C20 alkylamino; C1 -C20 aminoalkyl; substituted or unsubstituted phenyl or benzyl, the substituents being selected from hydroxy, fluorine, bromine, chlorine, C1 -C20 alkyl, C2 -C20 alkenyl, C2 -C20 (monohydroxy or polyhydroxy)alkyl, X is methyl or oxygen and n is 0 to 20. The invention is also directed to a method for increasing the topical penetration of a physiologically active agent across the skin or membrane of a mammalian organism. Also claimed is a pharmaceutical composition and a novel method for preparing 1-substituted-4-imidazolin-2-one.