Cas no 341006-18-6 (5-(Methoxymethoxy)-2-methylphenylboronic Acid)

5-(Methoxymethoxy)-2-methylphenylboronic acid is a boronic acid derivative commonly utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method for forming carbon-carbon bonds in organic synthesis. The methoxymethoxy (MOM) protecting group enhances stability while maintaining reactivity, making it particularly useful in multi-step synthetic routes. Its methyl substituent at the ortho position can influence steric and electronic properties, allowing for selective coupling in complex molecular frameworks. This compound is valuable in pharmaceutical and materials science research, where precise functionalization of aromatic systems is required. Proper handling under inert conditions is recommended to preserve its integrity.
5-(Methoxymethoxy)-2-methylphenylboronic Acid structure
341006-18-6 structure
Product Name:5-(Methoxymethoxy)-2-methylphenylboronic Acid
CAS No:341006-18-6
MF:C9H13BO4
MW:196.008123159409
MDL:MFCD11856010
CID:1083475
PubChem ID:22606938
Update Time:2025-06-13

5-(Methoxymethoxy)-2-methylphenylboronic Acid Chemical and Physical Properties

Names and Identifiers

    • (5-(Methoxymethoxy)-2-methylphenyl)boronic acid
    • 4-methoxymethoxy-1-methylbenzene-2-boronic acid
    • 5-(Methoxymethoxy)-2-methylphenylboronic acid
    • [5-(Methoxymethoxy)-2-methyl-phenyl]boronic acid
    • 341006-18-6
    • MFCD11856010
    • B-[5-(Methoxymethoxy)-2-methylphenyl]boronic acid
    • D71411
    • KXBXFELZYMVBDD-UHFFFAOYSA-N
    • DTXSID801234842
    • AKOS016016121
    • CS-0190029
    • [5-(methoxymethoxy)-2-methylphenyl]boronic acid
    • (5-(Methoxymethoxy)-2-methylphenyl)boronicacid
    • SCHEMBL6886441
    • DB-344750
    • 5-(Methoxymethoxy)-2-methylphenylboronic Acid
    • MDL: MFCD11856010
    • Inchi: 1S/C9H13BO4/c1-7-3-4-8(14-6-13-2)5-9(7)10(11)12/h3-5,11-12H,6H2,1-2H3
    • InChI Key: KXBXFELZYMVBDD-UHFFFAOYSA-N
    • SMILES: O(COC)C1C=CC(C)=C(B(O)O)C=1

Computed Properties

  • Exact Mass: 196.0906891g/mol
  • Monoisotopic Mass: 196.0906891g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 165
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 58.9?2

5-(Methoxymethoxy)-2-methylphenylboronic Acid Pricemore >>

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Additional information on 5-(Methoxymethoxy)-2-methylphenylboronic Acid

Comprehensive Overview of 5-(Methoxymethoxy)-2-methylphenylboronic Acid (CAS No. 341006-18-6)

5-(Methoxymethoxy)-2-methylphenylboronic Acid (CAS No. 341006-18-6) is a specialized boronic acid derivative widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound features a unique methoxymethoxy-protected phenol group, which enhances its stability and reactivity in various chemical transformations. Its molecular formula, C10H15BO4, and precise structure make it a valuable intermediate for pharmaceutical and materials science applications.

The growing demand for boronic acid-based reagents in drug discovery and agrochemical research has positioned 5-(Methoxymethoxy)-2-methylphenylboronic Acid as a critical building block. Researchers frequently search for "boronic acid derivatives for Suzuki coupling" or "protected phenol boronic acids," reflecting its relevance in modern synthetic chemistry. Its CAS No. 341006-18-6 is often queried in databases like SciFinder and Reaxys, underscoring its importance in high-impact research.

One of the standout features of this compound is its compatibility with green chemistry principles. As sustainability becomes a focal point in chemical manufacturing, 5-(Methoxymethoxy)-2-methylphenylboronic Acid is increasingly studied for its efficiency in minimizing waste and reducing hazardous byproducts. Searches for "eco-friendly boronic acid reagents" or "sustainable coupling reactions" align with these trends, highlighting its role in advancing greener methodologies.

In pharmaceutical applications, this boronic acid derivative is pivotal for constructing biaryl scaffolds, a common motif in drug candidates targeting inflammation, oncology, and CNS disorders. Queries such as "boronic acids in drug synthesis" or "methylphenylboronic acid applications" demonstrate its prominence in medicinal chemistry. The methoxymethoxy group further allows selective deprotection, enabling versatile synthetic routes.

From a commercial perspective, CAS No. 341006-18-6 is supplied by leading chemical vendors with high purity (>97%), catering to both academic and industrial labs. Its storage stability and solubility in common organic solvents (e.g., THF, DMSO) make it a practical choice for diverse reactions. Frequently searched terms like "buy 5-(Methoxymethoxy)-2-methylphenylboronic Acid" or "suppliers of boronic acid derivatives" reflect its market demand.

In summary, 5-(Methoxymethoxy)-2-methylphenylboronic Acid (CAS No. 341006-18-6) bridges innovation and practicality in synthetic chemistry. Its dual role in enabling complex molecular architectures and supporting sustainable practices ensures its continued relevance in cutting-edge research and industrial applications.

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