3613-97-6

Usage

Uses

Used in Agricultural Applications:
Phenoxyacetic N,N-diethylamide is used as a herbicide for controlling the growth of unwanted plants in agricultural fields. Its application reason is to disrupt the growth and metabolism of these plants, ultimately leading to their death and allowing for more efficient crop cultivation.
Used in Plant Growth Regulation:
Phenoxyacetic N,N-diethylamide is used as a plant growth regulator to manage the growth patterns of certain plants. Its application reason is to control the rate and direction of plant growth, which can be beneficial in horticulture and other plant-related industries.
Used in Industrial Applications:
Phenoxyacetic N,N-diethylamide is used in industrial settings for its herbicidal properties, particularly in areas where unwanted plant growth can cause issues or pose a risk to infrastructure. Its application reason is to prevent the growth of plants that could potentially damage or interfere with industrial operations.

InChI:InChI=1/C12H17NO2/c1-3-13(4-2)12(14)10-15-11-8-6-5-7-9-11/h5-9H,3-4,10H2,1-2H3

Upstream product

• 109-89-7 diethylamine 
• 701-99-5 Phenoxyacetyl chloride 
• 122-59-8 2-phenoxyacetic acid 
• 26578-64-3 1,1-bis(diethylamino)-2-chloroethene 
• 145303-94-2 1,1-bis(N,N-diethylamino)-2-phenoxyethylene 
• 109538-22-9 diethyl-(1,2-dichloro-vinyl)-amine 
• 139-02-6 sodium phenoxide 

Downstream Products

• 96823-01-7 3-phenoxy-7-methoxycoumarin 
• 114284-73-0 Diethyl-(7-phenoxy-[1,3]dioxolo[4,5-g]quinolin-6-yl)-amine 
• 78504-02-6 2-Chloro-4-phenoxymethyl-6-phenyl-[1,3,5]triazine 
• 2120-70-9 2-phenoxyethanal 
• 96823-00-6 8-Methoxy-3-phenoxy-chromen-2-one 
• 91787-19-8 3-phenoxy-2H-1-benzopyran-2-one 
• 42945-88-0 N,N-diethylphenoxythioacetamide 
• 96823-02-8 7-Methyl-3-phenoxy-chromen-2-one 
• 96823-03-9 6-Methyl-3-phenoxy-chromen-2-one 
• 96823-04-0 7-Phenoxy-[1,3]dioxolo[4,5-g]chromen-6-one 
• 63787-10-0 N,N-diethyl-4-(chloroacetyl)phenoxyacetamide 

Relevant academic research and scientific papers

A practical in situ generation of the schwartz reagent. reduction of tertiary amides to aldehydes and hydrozirconation

A new, highly efficient in situ protocol (Cp2ZrCl2/LiAlH(OBu-t)3) is described for the generation of the Schwartz reagent which provides a convenient method for the amide to aldehyde reduction and the regioselective hydrozirconation-iodination of alkynes and alkenes. Highlighted are chemoselective reductions of benzamides derived by directed ortho metalation (DoM) chemistry, allowing the synthesis of valuable 1,2,3-substituted benzaldehydes. The single-step, three-component process proceeds in a very short reaction time, shows excellent functional group compatibility, and uses inexpensive and long-storage stable reducing reagents.