60085-74-7

Basic information

• Product Name: (DIPHENYLAMINO)ACETIC ACID
• Synonyms: AKOS BBS-00000378;(DIPHENYLAMINO)ACETIC ACID;2-(DiphenylaMino)acetic acid
• CAS NO: 60085-74-7
• Molecular Formula: C₁₄H₁₃NO₂
• Molecular Weight: 227.26
• Mol File: 60085-74-7.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (DIPHENYLAMINO)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (DIPHENYLAMINO)ACETIC ACID(60085-74-7)
• EPA Substance Registry System: (DIPHENYLAMINO)ACETIC ACID(60085-74-7)

Safety Data

• Hazardous Substances Data: 60085-74-7(Hazardous Substances Data)

Usage

General Description

(DIPHENYLAMINO)ACETIC ACID, also known as fenoxycarb, is a chemical compound with the molecular formula C14H13NO2. It is a widely used pesticide and insecticide, particularly in agricultural settings. It works by interfering with the growth and reproduction of insects, ultimately leading to their death. It is often used to control pests such as aphids, caterpillars, and leafhoppers in crops such as cotton and rice. However, it is important to note that (DIPHENYLAMINO)ACETIC ACID can be toxic to aquatic organisms and should be handled and used with caution to avoid harm to the environment and non-target species.

Upstream product

• 122-39-4 diphenylamine 
• 598-21-0 2-Bromoacetyl bromide 
• 71086-42-5 N-(diphenylmethylene)glycine ethyl ester 
• 79-11-8 chloroacetic acid 

Downstream Products

• 866562-52-9 1-{4-[(3-chloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylamino-ethanone 
• 866562-53-0 1-{4-[(2-chloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylamino-ethanone 
• 866562-49-4 1-{4-[(2,4-dimethyl-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylamino-ethanone 
• 866562-54-1 1-{4-[(2,3-dichloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylamino-ethanone 
• 866562-50-7 1-{4-[(2,4-dichloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylamino-ethanone 
• 866562-48-3 1-(4-benzhydryl-piperazin-1-yl)-2-diphenylamino-ethanone 
• 1080623-42-2 ethyl 2-amino-2-(1-(3-chloro-4-fluorobenzyl)-2-oxo-3-(phenylsulfinyl)piperidin-4-yl)acetate 
• 60085-75-8 N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N,N-diphenylamino)acetamide 
• 165684-01-5 2-Diphenylamino-1-piperazin-1-yl-ethanone 
• 866562-51-8 1-{4-[(4-Chloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-2-diphenylaminoethanone 
• 158502-07-9 Diphenylamino-acetyl chloride 

Relevant articles and documents

Reagent-free continuous thermal tert-butyl ester deprotection

Continuous processing enables the use of non-standard reaction conditions such as high temperatures and pressures while in the liquid phase. This expands the chemist's toolbox and can enable previously unthinkable chemistry to proceed with ease. For a series of amphoteric amino acid derivatives, we have demonstrated the ability to hydrolyze the tert-butyl ester functionality in protic solvent systems. Using a continuous plug flow reactor at 120–240 °C and 15–40 min reaction times, no pH modification or additional reagents are needed to achieve the desired transformation. The method was then expanded to encompass a variety of more challenging substrates to test selectivity and racemization potential. The acid products were generally isolated as crystalline solids by simple solvent exchange after the deprotection reaction in good to high yield and purity.

Synthesis of some New Pharmacophores derived from Imidazole and Benzimidazole

-

Synthesis of Novel N-Substituted Phenothiazines and Piperazines as Potential Biologically Active Agents

-