10576-12-2 | Ethyl acetohydroximate

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$26.00	$18.00
5g	98%	in stock	$34.00	$24.00
25g	98%	in stock	$61.00	$43.00
100g	98%	in stock	$174.00	$122.00
500g	98%	in stock	$705.00	$494.00

Description

• Catalog Number: AE08269
• Chemical Name: Ethyl acetohydroximate
• CAS Number: 10576-12-2
• Molecular Formula: C4H9NO2
• Molecular Weight: 103.1198
• MDL Number: MFCD00002114
• SMILES: CC(=NO)OCC

Computed Properties

• Complexity: 70.1
• Covalently-Bonded Unit Count: 1
• Defined Bond Stereocenter Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.7

Upstream Synthesis Route

Ethyl N-hydroxyacetimidate is a versatile chemical reagent commonly used in organic synthesis due to its ability to serve as a valuable precursor in various reactions. This compound is particularly valued in the field of chemical synthesis for its role in facilitating the formation of carbon-carbon, carbon-oxygen, and carbon-nitrogen bonds.In organic chemistry, Ethyl N-hydroxyacetimidate is frequently employed as a key reagent in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and natural products. It plays a crucial role in the construction of molecular frameworks by enabling the selective introduction of functional groups at specific sites on the target molecule. Additionally, Ethyl N-hydroxyacetimidate can participate in a range of transformation reactions, offering chemists precise control over the structural modifications of organic compounds.Furthermore, the unique properties of Ethyl N-hydroxyacetimidate allow for efficient and selective reactions, making it a valuable tool for chemists seeking to streamline synthetic processes and improve product yields. Its versatility and reliability make it a preferred reagent for researchers and professionals in the chemical industry striving to optimize the synthesis of novel compounds with diverse applications.

Literature

• Pd-catalyzed O-arylation of ethyl acetohydroximate: synthesis of O-arylhydroxylamines and substituted benzofurans.

  Journal of the American Chemical Society 20100728