1245816-10-7 | 5-Methyl-1H-indazol-4-yl boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$6.00	$5.00
1g	98%	in stock	$12.00	$9.00
5g	98%	in stock	$46.00	$33.00
10g	98%	in stock	$91.00	$64.00
25g	98%	in stock	$193.00	$135.00

Description

• Catalog Number: AA28860
• Chemical Name: 5-Methyl-1H-indazol-4-yl boronic acid
• CAS Number: 1245816-10-7
• Molecular Formula: C8H9BN2O2
• Molecular Weight: 175.9803
• MDL Number: MFCD10001490
• SMILES: OB(c1c(C)ccc2c1cn[nH]2)O

Computed Properties

• Complexity: 191
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

The (5-methyl-1H-indazol-4-yl)boronic acid is a versatile building block commonly used in chemical synthesis as a key component for constructing complex organic molecules. This compound is widely utilized in modern synthetic chemistry due to its ability to serve as a vital precursor in numerous organic reactions, particularly in the field of metal-catalyzed cross-coupling reactions.In the realm of chemical synthesis, (5-methyl-1H-indazol-4-yl)boronic acid plays a crucial role in the formation of carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds through a variety of coupling reactions. By acting as a boronate ester, this compound can undergo Suzuki-Miyaura coupling, Stille coupling, Chan-Lam coupling, and other palladium-catalyzed cross-coupling reactions to link with various organic substrates.Moreover, the unique structural characteristics of (5-methyl-1H-indazol-4-yl)boronic acid enable chemists to introduce specific functionalities or motifs into target molecules with precision. This compound's compatibility with various functional groups and its high reactivity make it a valuable tool for synthesizing pharmaceuticals, agrochemicals, materials, and other biologically active compounds with tailored properties.Overall, the utility of (5-methyl-1H-indazol-4-yl)boronic acid in chemical synthesis lies in its ability to facilitate the efficient, selective, and controlled construction of diverse organic molecules with enhanced structural complexity and functionality.