122-28-1 | 3'-Nitroacetanilide

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$15.00	$10.00
1g	98%	in stock	$19.00	$13.00
5g	98%	in stock	$38.00	$26.00
25g	98%	in stock	$68.00	$48.00
500g	98%	in stock	$1,171.00	$820.00

Description

• Catalog Number: AB65432
• Chemical Name: 3'-Nitroacetanilide
• CAS Number: 122-28-1
• Molecular Formula: C8H8N2O3
• Molecular Weight: 180.1607
• MDL Number: MFCD00017015
• SMILES: CC(=O)Nc1cccc(c1)[N+](=O)[O-]

Computed Properties

• Complexity: 212
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.5

Upstream Synthesis Route

N-(3-Nitrophenyl)acetamide, commonly referred to as $name$, is a versatile compound that finds wide application in chemical synthesis processes. This compound serves as a crucial building block in the creation of various organic molecules due to its unique reactivity and functional groups.One key application of $name$ in chemical synthesis is its use as a starting material for the synthesis of pharmaceuticals and agrochemicals. By incorporating this compound into the synthesis pathway, chemists can introduce the 3-nitrophenyl group and acetamide moiety into the target molecule, imparting specific chemical properties and biological activities.Additionally, $name$ is utilized as a reagent in the preparation of heterocyclic compounds, which are vital in the development of new materials, dyes, and bioactive molecules. The nitro group in the 3-nitrophenyl ring can undergo various transformations, enabling the creation of diverse chemical structures with desired properties.Furthermore, in the field of organic synthesis, N-(3-Nitrophenyl)acetamide serves as a valuable tool for the construction of complex molecules through multi-step reactions. Its compatibility with a range of synthetic methods allows for efficient and controlled manipulation of chemical bonds, enabling chemists to access a wide array of structurally diverse compounds.Overall, the versatile nature of N-(3-Nitrophenyl)acetamide makes it an indispensable component in the toolkit of synthetic chemists, facilitating the development of innovative and functional materials for various applications.

Literature

• Kinetic analysis of butyrylcholinesterase-catalyzed hydrolysis of acetanilides.

  Biochimica et biophysica acta 20070901

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501