17484-36-5 | 4-Methyl-3-nitroanisole

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
5g	98%	in stock	$32.00	$22.00
10g	98%	in stock	$40.00	$28.00
25g	98%	in stock	$65.00	$45.00
100g	98%	in stock	$250.00	$175.00

Description

• Catalog Number: AA93103
• Chemical Name: 4-Methyl-3-nitroanisole
• CAS Number: 17484-36-5
• Molecular Formula: C8H9NO3
• Molecular Weight: 167.162
• MDL Number: MFCD00007173
• SMILES: COc1ccc(c(c1)[N+](=O)[O-])C

Computed Properties

• Complexity: 166
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

4-Methyl-3-nitroanisole, also known as 4-methoxy-3-nitrotoluene, is a versatile compound widely used in chemical synthesis. One of its key applications is as a building block in the synthesis of various organic compounds. This compound serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 4-Methyl-3-nitroanisole can be utilized as a precursor for creating more complex molecules through substitution, reduction, or other chemical reactions. Its nitro and methoxy functional groups make it a valuable starting material for synthesizing a range of diverse compounds with unique properties and functionalities. The compound's structure and reactivity make it particularly valuable in the design and production of specialty chemicals and intermediates for the pharmaceutical industry.Moreover, 4-Methyl-3-nitroanisole can be employed in the synthesis of dyes, fragrances, and other specialty chemicals that require precise control over the substitution patterns and molecular structures. Its versatile nature and ability to undergo various chemical transformations make it a valuable tool for organic chemists seeking to tailor molecules for specific applications. In summary, 4-Methyl-3-nitroanisole plays a crucial role in chemical synthesis by serving as a key building block for the creation of diverse organic compounds with varied industrial applications.

Literature

• Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides.

  Chemical communications (Cambridge, England) 20060414

• Synthesis and evaluation of 5,7-dihydro-3-[2-[1-(4-[18F]-fluorobenzyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one for in vivo mapping of acetylcholinesterase.

  Nuclear medicine communications 20040601