1000801-76-2 | 1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$24.00	$17.00
5g	98%	in stock	$109.00	$77.00
10g	98%	in stock	$218.00	$153.00

Description

• Catalog Number: AA00929
• Chemical Name: 1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole
• CAS Number: 1000801-76-2
• Molecular Formula: C13H23BN2O3
• Molecular Weight: 266.1443
• MDL Number: MFCD16659789
• SMILES: COCCCn1ncc(c1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 296
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5

Upstream Synthesis Route

1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in organic chemistry as a key building block for the creation of various functional molecules. Its unique structure allows for selective reactions to take place, enabling chemists to access complex structures efficiently.In chemical synthesis, $name$ is often employed as a reagent for cross-coupling reactions, specifically in Suzuki-Miyaura couplings. This process involves the coupling of an aryl or vinyl halide with an organoboron compound, typically facilitated by a palladium catalyst. $name$ serves as the boron-containing component in these transformations, participating in the formation of new carbon-carbon bonds with high efficiency and selectivity.Furthermore, $name$ can also be utilized in the synthesis of heterocyclic compounds, offering a strategic approach to access diverse chemical structures with desired properties. Its use in the construction of pyrazole derivatives, for instance, allows for the preparation of compounds with potential biological activities or unique physicochemical properties.Overall, the application of 1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in chemical synthesis showcases its significance as a valuable tool for the development of novel molecules and the advancement of synthetic methodologies.