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52107-90-1

3-IODO-5-METHYL-BENZOIC ACID

Catalog#: AR00DZNU  |   CAS#: 52107-90-1  |   MDL#: MFCD11007824  |   MF: C8H7IO2  |   MW: 262.0444

Packsize Purity Price Availability Quantity
100mg 95% $33.00 Global Stock Buy Now Add To Cart
250mg 95% $55.00 Global Stock Buy Now Add To Cart
1g 95% $148.00 Global Stock Buy Now Add To Cart
5g 95% $650.00 Global Stock Buy Now Add To Cart
10g 95% $1,226.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DZNU
Chemical Name 3-IODO-5-METHYL-BENZOIC ACID
CAS Number 52107-90-1
Molecular Formula C8H7IO2
Molecular Weight 262.0444
MDL Number MFCD11007824
SMILES Cc1cc(I)cc(c1)C(=O)O

3-Iodo-5-methylbenzoic acid, also known as meta-iodo-m-xylene-carboxylic acid, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it an essential building block in various organic reactions and transformations. In particular, this compound is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.One of the key applications of 3-Iodo-5-methylbenzoic acid is as a precursor in the preparation of biologically active molecules. Its iodine substituent serves as a valuable handle for further functionalization, allowing for the introduction of diverse chemical groups to modulate the properties of the final product. Additionally, the methyl group at the 5-position provides steric protection and can influence the reactivity and selectivity of subsequent reactions.In chemical synthesis, 3-Iodo-5-methylbenzoic acid can participate in various transformations such as cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations. By judiciously selecting reaction conditions and reagents, chemists can leverage the unique reactivity of this compound to access a wide range of structurally complex and pharmacologically relevant molecules.Overall, the multifaceted nature of 3-Iodo-5-methylbenzoic acid makes it a valuable tool for synthetic chemists seeking to access novel chemical entities for pharmaceutical and materials science applications. Its strategic placement of functional groups and its reactivity profile make it a versatile and powerful building block for diverse chemical transformations.
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