108078-14-4 | 2-Iodo-3-methylbenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$11.00	$8.00
5g	97%	in stock	$15.00	$11.00
10g	97%	in stock	$18.00	$13.00
25g	97%	in stock	$22.00	$16.00

Description

• Catalog Number: AB62393
• Chemical Name: 2-Iodo-3-methylbenzoic acid
• CAS Number: 108078-14-4
• Molecular Formula: C8H7IO2
• Molecular Weight: 262.0444
• MDL Number: MFCD00079764
• SMILES: OC(=O)c1cccc(c1I)C

Computed Properties

• Complexity: 158
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.5

Upstream Synthesis Route

2-Iodo-3-methylbenzoic acid is a versatile compound widely used in chemical synthesis. Its unique chemical structure provides valuable opportunities for various applications in the field of organic chemistry. One of the key applications of 2-Iodo-3-methylbenzoic acid is its use as a building block in the synthesis of pharmaceutical intermediates. Its iodo and carboxylic acid functional groups make it a valuable precursor for the creation of complex molecules with potential biological activity. Researchers utilize this compound to introduce specific functional groups into target molecules, allowing for the synthesis of novel drug candidates and potential therapeutics.Furthermore, 2-Iodo-3-methylbenzoic acid serves as a valuable tool in the field of materials science. Its ability to undergo various chemical transformations enables the generation of specialized materials with tailored properties. By incorporating this compound into polymerization reactions, researchers can create polymers with specific functional groups or structures, enhancing their performance in various applications such as coatings, adhesives, or advanced materials.In summary, the versatile nature of 2-Iodo-3-methylbenzoic acid makes it a valuable reagent in chemical synthesis, particularly in the development of pharmaceutical intermediates and specialized materials for a wide range of applications.

Literature

• New substituted isocoumarins and Dihydroisocoumarins and their cytotoxic activities.

  Scientia pharmaceutica 20110101