10397-30-5 | 4-Methyl-3-nitrobenzoyl chloride

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$25.00	$17.00
25g	98%	in stock	$58.00	$41.00
100g	98%	in stock	$169.00	$118.00

Description

• Catalog Number: AB67948
• Chemical Name: 4-Methyl-3-nitrobenzoyl chloride
• CAS Number: 10397-30-5
• Molecular Formula: C8H6ClNO3
• Molecular Weight: 199.59114
• MDL Number: MFCD00035747
• SMILES: [O-][N+](=O)c1cc(ccc1C)C(=O)Cl

Computed Properties

• Complexity: 226
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2.9

Upstream Synthesis Route

4-Methyl-3-nitrobenzoyl chloride, also known as MNBC, is a versatile compound widely used in organic synthesis. This compound plays a crucial role in various chemical reactions due to its unique reactivity and structural properties. In chemical synthesis, 4-Methyl-3-nitrobenzoyl chloride serves as a key building block for the preparation of diverse organic compounds.One of the primary applications of 4-Methyl-3-nitrobenzoyl chloride is as an acylating agent in Friedel-Crafts acylation reactions. This compound can react with various nucleophiles, such as aromatic compounds or amines, to introduce the 4-Methyl-3-nitrobenzoyl group into the target molecule. This acylation process is essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.Additionally, 4-Methyl-3-nitrobenzoyl chloride is also utilized in the preparation of heterocyclic compounds through cyclization reactions. By reacting with suitable nucleophiles or substrates, this compound can facilitate the formation of diverse heterocyclic rings, which are prevalent in medicinal chemistry and materials science.Moreover, 4-Methyl-3-nitrobenzoyl chloride can be employed in the synthesis of various dyes, pigments, and polymers. Its reactivity allows for the functionalization of aromatic rings, enabling the creation of complex molecular structures with specific properties and functionalities.Overall, the versatility and reactivity of 4-Methyl-3-nitrobenzoyl chloride make it a valuable reagent in chemical synthesis, offering numerous opportunities for the design and preparation of novel organic compounds with diverse applications in the fields of pharmaceuticals, materials science, and agrochemicals.