698357-97-0

Basic information

• Product Name: 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE
• Synonyms: 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE;2-[2-(2,6-Dichloro-phenylamino)-5-hydroxy-phenyl]-N,N-dimethylacetamide;2-[(2,6-Dichlorophenyl)aMino]-5-hydroxy-N,N-diMethyl-benzeneacetaMide
• CAS NO: 698357-97-0
• Molecular Formula: C₁₆H₁₆Cl₂N₂O₂
• Molecular Weight: 339.21644
• Product Categories: Amines;Aromatics
• Mol File: 698357-97-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Solubility: Chloroform, Ethyl Acetate, Ethyl Ether,
• CAS DataBase Reference: 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE(698357-97-0)
• EPA Substance Registry System: 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE(698357-97-0)

Safety Data

• Hazardous Substances Data: 698357-97-0(Hazardous Substances Data)

Usage

Description

2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE, with the chemical abstracts service number 698357-97-0, is a specialized organic compound that plays a significant role in the field of organic synthesis. Its unique molecular structure, featuring a dichlorophenyl-amino group and a hydroxyphenyl moiety, endows it with specific chemical properties that are valuable for creating a variety of complex organic molecules.

Uses

Used in Organic Synthesis:
2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE is used as a key intermediate in the synthesis of various organic compounds. Its presence in reactions can facilitate the formation of desired products by providing a reactive site for further functionalization or by acting as a protecting group for sensitive functional groups during the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE is utilized as a building block for the development of new drugs. Its unique structural features can be incorporated into drug molecules to enhance their pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Chemical Research:
2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE also serves as a valuable tool in chemical research, where it can be used to study reaction mechanisms, explore new synthetic methodologies, and investigate the properties of novel chemical entities.
Used in Material Science:
In the field of material science, 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE can be employed in the design and synthesis of advanced materials with specific properties, such as high thermal stability, unique optical characteristics, or improved mechanical strength.
Each of these applications highlights the versatility and importance of 2-[(2',6'-DICHLOROPHENYL)AMINO]-5-HYDROXYPHENYL-N,N-DIMETHYLACETAMIDE in various scientific and industrial domains, underscoring its potential to contribute to the advancement of chemical knowledge and the development of innovative products.

Upstream product

• 99540-20-2 (6-iodo-3-methoxy)phenyl-N,N-dimethylacetamide 
• 90526-08-2 2-(3-methoxyphenyl)-N,N-dimethylacetamide 
• 698357-92-5 2-[(2',6'-dichlorophenyl)amino]-5-methoxyphenyl-N,N-dimethylacetamide 

Downstream Products

• 69002-84-2 2-(2-((2,6-dichlorophenyl)amino)-5-hydroxyphenyl)acetic acid 

Relevant articles and documents

Syntheses and characterization of the acyl glucuronide and hydroxy metabolites of diclofenac

In humans, metabolism of the commonly used nonsteroidal antiinflammatory drug diclofenac 1 yields principally the 4′-hydroxy 2, 5-hydroxy 3, and acyl glucuronide 4 metabolites. All three metabolites have been implicated in rare idiosyncratic adverse react