1182283-83-5 | (4-(3-Chloropropoxy)phenyl)boronic acid

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	2 weeks	$105.00	$73.00
2mg	95%	2 weeks	$123.00	$86.00
3mg	95%	2 weeks	$149.00	$105.00
5mg	95%	2 weeks	$168.00	$118.00
10mg	95%	2 weeks	$193.00	$135.00
100mg	95%	2 weeks	$399.00	$279.00
250mg	95%	2 weeks	$713.00	$499.00
500mg	95%	2 weeks	$993.00	$695.00
1g	95%	2 weeks	$1,412.00	$988.00

Description

• Catalog Number: AE26829
• Chemical Name: (4-(3-Chloropropoxy)phenyl)boronic acid
• CAS Number: 1182283-83-5
• Molecular Formula: C9H12BClO3
• Molecular Weight: 214.4538
• MDL Number: MFCD28384317
• SMILES: ClCCCOc1ccc(cc1)B(O)O

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5

Upstream Synthesis Route

(4-(3-chloropropoxy)phenyl)boronic acid, also known as $name$, is a highly versatile and valuable compound in the field of chemical synthesis. This compound serves as a crucial building block in the creation of various organic molecules and plays a vital role in the development of new materials and pharmaceuticals.In chemical synthesis, (4-(3-chloropropoxy)phenyl)boronic acid is frequently utilized as a key reagent in Suzuki-Miyaura cross-coupling reactions. This important reaction enables the formation of carbon-carbon bonds, allowing for the efficient and selective assembly of complex organic structures. By acting as a boronic acid derivative, (4-(3-chloropropoxy)phenyl)boronic acid serves as a nucleophilic partner in the cross-coupling process, facilitating the connection of diverse functional groups and substrates.Moreover, the presence of the chloro and alkoxy groups in (4-(3-chloropropoxy)phenyl)boronic acid provides additional synthetic possibilities, allowing for fine-tuning of reactivity and selectivity in chemical transformations. This enables chemists to access a wide range of chemical space and design molecules with tailored properties for specific applications.Overall, the strategic incorporation of (4-(3-chloropropoxy)phenyl)boronic acid in chemical synthesis not only enhances the efficiency and selectivity of reactions but also opens up new avenues for the synthesis of intricate organic molecules with diverse functionalities.