7509-61-7

Basic information

• Product Name: (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide
• Synonyms: (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide;(2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)ethanamide;(2E)-N-(2-ethylphenyl)-2-hydroximino-acetamide;(2E)-N-(2-ethylphenyl)-2-hydroxyimino-ethanamide;Acetamide, 2-hydroximino-N-(2-ethylphenyl)-;N-(2-ethylphenyl)-2-hydroximino-acetamide;N-(2-ethylphenyl)-2-hydroxyiminoacetamide;N-(2-ethylphenyl)-2-hydroxyimino-acetamide
• CAS NO: 7509-61-7
• Molecular Formula: C₁₀H₁₂N₂O₂
• Molecular Weight: 192.21448
• Mol File: 7509-61-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.14g/cm³
• Refractive Index: 1.551
• CAS DataBase Reference: (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide(7509-61-7)
• EPA Substance Registry System: (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide(7509-61-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 7509-61-7(Hazardous Substances Data)

Usage

General Description

(2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide is an organic compound with the molecular formula C12H15NO2. It is a member of the hydroxylamine family and is commonly used in the field of organic synthesis. This chemical is a white to off-white crystalline powder that is soluble in organic solvents such as methanol and ethanol. It is often employed as a reagent in the preparation of various organic compounds due to its ability to act as a versatile precursor for the synthesis of different functional groups. Additionally, it can also be utilized as a building block for the creation of heterocyclic compounds and other biologically active molecules.

InChI:InChI=1/C10H12N2O2/c1-2-8-5-3-4-6-9(8)12-10(13)7-11-14/h3-7,14H,2H2,1H3,(H,12,13)

Upstream product

• 302-17-0 chloral hydrate 
• 578-54-1 ortho-ethylaniline 

Downstream Products

• 79183-65-6 7-ethylisatin 
• 5437-40-1 2-amino-3-ethylbenzoic acid 
• 1067186-32-6 8-ethyl-3-hydroxy-2-(1-phenylcyclopropyl)quinoline-4-carboxylic acid 

Relevant articles and documents

Palladium(II)/N-Heterocyclic Carbene Catalyzed One-Pot Sequential α-Arylation/Alkylation: Access to 3,3-Disubstituted Oxindoles

Rationally designed fluorene-based mono- and bimetallic Pd-PEPPSI complexes were synthesized and demonstrated to be effective for the one-pot sequential α-arylation/alkylation of oxindoles. This streamlined approach offers efficient access to functionalized 3,3-disubstituted oxindoles in excellent yields (up to 89%) under mild reaction conditions.

Methods and Compositions for Selectin Inhibition

The present teachings relate to novel compounds of formula I: wherein the constituent variables are as defined herein. Compounds of the present teachings can act as antagonists of the mammalian adhesion proteins known as selecting. Methods for treating or preventing selectin-mediated disorders are provided, which include administration of these compounds in a therapeutically effective amount.

Condensed bridgehead nitrogen heterocyclic systems: Synthesis and antimicrobial activity of thiazolo[3′, 2′: 2, 3]-as-triazino[5, 6-b]indoles and isomeric thiazolo[2′, 3′: 3, 4]-as-triazino[5, 6-b]indoles

2, 3-Dihydro-6-ethyl-5H-as-triazino[5, 6-b]indole-3-thione 4 on condensation with α-haloketone gives 3-aroylmethylthio-6-ethyl-5H-as-triazino[5, 6-b]indolehydrobromide 5 which on PPA catalyzed cyclization furnishes 3-aryl-9-ethylthiazolo[3′, 2′: 2, 3]-as-