2483-57-0 | Methyl nitroacetate

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$16.00	$12.00
10g	97%	in stock	$30.00	$21.00
25g	97%	in stock	$65.00	$45.00
100g	97%	in stock	$186.00	$130.00

Description

• Catalog Number: AB26293
• Chemical Name: Methyl nitroacetate
• CAS Number: 2483-57-0
• Molecular Formula: C3H5NO4
• Molecular Weight: 119.0761
• MDL Number: MFCD00075480
• SMILES: [O-][N+](=O)CC(=O)OC
• NSC Number: 16153

Computed Properties

• Complexity: 104
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• XLogP3: 0.1

Upstream Synthesis Route

Methyl Nitroacetate is a versatile chemical compound that finds wide application in organic synthesis processes. With its unique chemical properties, Methyl Nitroacetate serves as a valuable building block in the creation of various complex molecules, making it a valuable tool for chemists in the laboratory.In chemical synthesis, Methyl Nitroacetate is commonly used as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its nitro group can undergo various reactions such as reduction, substitution, and addition, allowing for the introduction of different functional groups into the molecule. This flexibility makes Methyl Nitroacetate an essential component in the synthesis of a wide range of organic compounds.Additionally, Methyl Nitroacetate can participate in specific reactions like Michael additions, acylations, and condensations, enabling chemists to construct complex molecular structures efficiently. By incorporating Methyl Nitroacetate into their synthetic routes, researchers can access diverse chemical functionalities and create novel compounds with tailored properties for various applications.Overall, the use of Methyl Nitroacetate in chemical synthesis showcases its significance as a valuable reagent that enables the efficient and strategic construction of intricate organic molecules for medicinal, agricultural, and industrial purposes.

Literature

• Catalytic intermolecular allylic C-H alkylation.

  Journal of the American Chemical Society 20081029

• Expedient synthesis of cyclopropane alpha-amino acids by the catalytic asymmetric cyclopropanation of alkenes using iodonium ylides derived from methyl nitroacetate.

  Journal of the American Chemical Society 20051228