33108-89-3

Basic information

• Product Name: (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride
• CAS NO: 33108-89-3
• Molecular Formula: C₉H₈ClNO₂
• Molecular Weight: 197.6183
• Mol File: 33108-89-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 356.434°C at 760 mmHg
• Flash Point: 169.366°C
• Density: 1.262g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.56
• CAS DataBase Reference: (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride(33108-89-3)
• EPA Substance Registry System: (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride(33108-89-3)

Safety Data

• Hazardous Substances Data: 33108-89-3(Hazardous Substances Data)

Usage

Description

(1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride is an organic compound belonging to the imidoyl chloride family, characterized by its molecular formula C9H8ClNO2. It features a hydroxy group and a methylphenyl group, which contribute to its versatile reactivity. (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride is recognized for its potential in organic synthesis, medicinal chemistry, and drug design due to its ability to engage with biological targets. Its unique chemical properties also render it valuable in a range of chemical reactions and processes.

Uses

Used in Organic Synthesis:
(1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride serves as a key intermediate in organic synthesis, facilitating the creation of complex molecular structures. Its reactivity allows for the formation of various chemical bonds, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride is utilized as a building block for the development of new drugs. Its capacity to interact with biological targets makes it a promising candidate for the design of molecules with therapeutic potential.
Used in Drug Design and Development:
(1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride is employed as a structural element in drug design and development. Its presence in a molecule can influence the pharmacokinetic and pharmacodynamic properties, contributing to the overall effectiveness and safety of a drug.
Used in Chemical Reactions and Processes:
(1Z)-N-hydroxy-2-(4-methylphenyl)-2-oxoethanimidoyl chloride is also used in various chemical reactions and processes outside of the pharmaceutical industry. Its unique properties enable it to participate in a wide array of transformations, making it a versatile tool in the chemical industry for the production of diverse chemical products.

Upstream product

• 544-16-1 n-Butyl nitrite 
• 4209-24-9 p-methylphenacyl chloride 
• 122-00-9 para-methylacetophenone 
• 17628-76-1 p-tolylglyoxalmonoxime 

Downstream Products

• 68659-06-3 C,C'-di-p-tolyl-C,C'-isoxazole-3,5-diyl-bis-methanone 
• 68659-12-1 C'-(4-bromo-phenyl)-C-p-tolyl-C,C'-isoxazole-3,5-diyl-bis-methanone 
• 102356-84-3 4-[3-(4-toluoyl)isoxazol-5-yl]butan-1-ol 
• 1100744-79-3 4-(5-methyl-1-phenyl-1H-pyrazol-4-carbonyl)-3-(4-methylbenzoyl)isoxazole 
• 102252-38-0 isopropyl [3-(4-toluoyl)-1,2,4-oxadiazol-5-yl]acetate 
• 102252-33-5 [3-(4-Toluoyl)-1,2,4-oxadiazol-5-yl]acetamide 
• 102252-43-7 [3-(4-toluoyl)-1,2,4-oxadiazol-5-yl]acetic acid 
• 102356-78-5 2-[3-(4-toluoyl)isoxazol-5-yl]ethanol 
• 102941-51-5 S-2-(N,N-dimethylamino)ethyl (4'-methylbenzoyl)thioformohydroximate 
• 58144-64-2 (4-methylphenyl)(5-phenyl-1,2-oxazol-3-yl)methanone 
• 143962-59-8 chloro-p-tolylglyoxime 
• 53360-85-3 2-amino-1-(4-methylphenyl)ethanol 
• 99-94-5 p-Toluic acid 

Relevant articles and documents

Aroylnitrile oxide cyclizations. 1. Synthesis of (3-aroyl-1,2,4-oxadiazol-5-yl)acetic acids

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