103-89-9 | 4'-Methylacetanilide

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$14.00	$10.00
25g	95%	in stock	$25.00	$18.00
100g	95%	in stock	$66.00	$47.00
500g	95%	in stock	$255.00	$179.00

Description

• Catalog Number: AB45088
• Chemical Name: 4'-Methylacetanilide
• CAS Number: 103-89-9
• Molecular Formula: C9H11NO
• Molecular Weight: 149.1897
• MDL Number: MFCD00008677
• SMILES: CC(=O)Nc1ccc(cc1)C
• NSC Number: 7644

Computed Properties

• Complexity: 137
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

4'-Methylacetanilide, also known as N-methyl-4-acetanilide, is a valuable compound widely utilized in chemical synthesis. This versatile chemical serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and dyes. Its unique structure and reactivity make it an essential intermediate in organic chemistry processes.In chemical synthesis, 4'-Methylacetanilide is commonly employed as a precursor in the creation of complex molecules due to its ability to undergo various transformations. Its substitution pattern and functional groups enable the introduction of additional chemical moieties, allowing for the modification of molecular properties and the enhancement of desired characteristics.Furthermore, 4'-Methylacetanilide plays a significant role in the development of novel drug candidates and fine chemicals. Its presence in organic reactions contributes to the synthesis of diverse compounds with potential applications in the pharmaceutical industry. By serving as a key starting material, this compound facilitates the construction of intricate molecular structures with specific biological activities.Overall, the strategic utilization of 4'-Methylacetanilide in chemical synthesis showcases its importance as a valuable component in the creation of advanced materials and compounds. With its crucial role in organic transformations and product diversification, this compound continues to be an indispensable asset in the field of chemistry.

Literature

• H/D isotopic recognition mechanism in hydrogen-bonded crystals of 3-methylacetanilide and 4-methylacetanilide.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20121101

• Ru (III) catalyzed oxidation of aliphatic ketones by N-bromosuccinimide in aqueous acetic acid: a kinetic study.

  TheScientificWorldJournal 20120101

• 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

• Structural properties of benzimidazole cavitand and its selective recognition toward 4-methylbenzamide over 4-methylanilide.

  The Journal of organic chemistry 20050722