13246-96-3

Basic information

• Product Name: 2-(2,4-dichlorophenoxy)-N-phenylacetamide
• Synonyms: 2-(2,4-Dichlorophenoxy)-N-phenylacetamide; Acetamide, 2-(2,4-dichlorophenoxy)-N-phenyl-
• CAS NO: 13246-96-3
• Molecular Formula: C₁₄H₁₁Cl₂NO₂
• Molecular Weight: 296.1486
• Mol File: 13246-96-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 497.5°C at 760 mmHg
• Flash Point: 254.7°C
• Density: 1.378g/cm³
• Vapor Pressure: 4.94E-10mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 2-(2,4-dichlorophenoxy)-N-phenylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-dichlorophenoxy)-N-phenylacetamide(13246-96-3)
• EPA Substance Registry System: 2-(2,4-dichlorophenoxy)-N-phenylacetamide(13246-96-3)

Safety Data

• Hazardous Substances Data: 13246-96-3(Hazardous Substances Data)

Usage

Usage

Herbicide

Target

Broadleaf weeds in crops such as corn, soybeans, and cereals

Mechanism of Action

Inhibits growth by disrupting hormone balance in target plants

Mammalian Toxicity

Low

Safety in Agriculture

Relatively safe when used according to label instructions

Precaution

Potential harmful effects on human health with prolonged or high-level exposure

Upstream product

• 94-75-7 2,4-Dichlorophenoxyacetic acid 
• 62-53-3 aniline 
• 774-74-3 2-(2,4-dichlorophenoxy)acetyl chloride 
• 5625-99-0 N,N'-diphenylphosphorodiamidic chloride 
• 13241-78-6 1-[(2,4-dichloro-phenoxy)-acetyl]-3,5-dimethyl-1H-pyrazole 
• 626239-03-0 N-(2,4-dichloro-phenyl)-2-hydroxy-N-phenyl-acetamide 
• 58373-59-4 2,4-dichloro-N-phenylaniline 
• 626239-02-9 2-Chloro-N-(2,4-dichloro-phenyl)-N-phenyl-acetamide 

Downstream Products

• 89565-65-1 N⁴-(2',4'-Dichlorophenoxyacetyl)sulfanilyl chloride 
• 94026-10-5 N-Methyl-N-phenyl-2,4-dichlor-phenoxy-acetamid 
• 575-90-6 2,6-dichlorophenoxyacetic acid 
• 58373-59-4 2,4-dichloro-N-phenylaniline 
• 89565-58-2 N⁴-(2',4'-Dichlorophenoxyacetyl)-N,N-dimethylsulfanilamide 
• 89565-59-3 C₁₄H₁₃Cl₂N₃O₄S 
• 89565-60-6 C₁₇H₁₇Cl₂N₃O₄S 
• 89565-61-7 2-(2,4-Dichloro-phenoxy)-N-[4-(morpholine-4-sulfonyl)-phenyl]-acetamide 
• 89565-63-9 C₂₀H₂₅Cl₂N₂O₇PS 

Relevant articles and documents

A convenient preparation of N-alkyl and N-arylamines by smiles rearrangement - Synthesis of analogues of diclofenac

Smiles rearrangement of substituted aryloxyacetamides in which oxygen and nitrogen are separated by COCH2 group has been successful even when the aryloxy ring carries weak or no electron withdrawing group. Earlier reports of such reactions involved either strong electron withdrawing groups or a special catalyst. The diphenylamines thus obtained gave analogues of diclofenac in only one case.

Studies on herbicides and plant growth regulators. II. Synthesis and some reactions of 1-aryloxyacylpyrazoles.

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