1050510-36-5 | 2-(Cyclopropylmethoxy)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$299.00	$209.00
5g	96%	in stock	$760.00	$532.00
10g	96%	in stock	$1,179.00	$825.00

Description

• Catalog Number: AD69338
• Chemical Name: 2-(Cyclopropylmethoxy)phenylboronic acid
• CAS Number: 1050510-36-5
• Molecular Formula: C10H13BO3
• Molecular Weight: 192.0194
• MDL Number: MFCD04039015
• SMILES: OB(c1ccccc1OCC1CC1)O

Computed Properties

• Complexity: 182
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Upstream Synthesis Route

The (2-(Cyclopropylmethoxy)phenyl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. Its unique structure, containing a boronic acid group attached to a phenyl ring with a cyclopropylmethoxy moiety, lends itself to various applications in chemical transformations. This compound is often utilized as a robust building block for constructing complex molecules in medicinal chemistry and material science. One of the key uses of (2-(Cyclopropylmethoxy)phenyl)boronic acid is its ability to participate in Suzuki-Miyaura cross-coupling reactions, a powerful method for forming carbon-carbon bonds. By reacting with aryl halides or pseudohalides in the presence of a palladium catalyst, this boronic acid derivative can facilitate the synthesis of biaryl compounds, which are prevalent in pharmaceuticals and agrochemicals.Additionally, (2-(Cyclopropylmethoxy)phenyl)boronic acid can serve as a valuable tool in the development of functional materials such as liquid crystals, polymers, and organic electronics. Its boronic acid functionality enables it to engage in selective recognition and binding with specific molecules or surfaces, making it instrumental in the preparation of sensor materials, molecular switches, and supramolecular assemblies.In summary, the (2-(Cyclopropylmethoxy)phenyl)boronic acid plays a crucial role in modern chemical synthesis by enabling the efficient construction of intricate molecular architectures and functional materials through Suzuki-Miyaura cross-coupling reactions and molecular recognition pathways. Its diverse applications highlight its significance in advancing the field of organic chemistry and materials science.

Literature

• Mirfentanil and A-4334: Tritiation at high specific activity.

  Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine 20100101