152626-78-3 | 5-Bromo-6-methoxy-1H-indazole

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$12.00
5g	98%	in stock	$76.00	$54.00

Description

• Catalog Number: AB45249
• Chemical Name: 5-Bromo-6-methoxy-1H-indazole
• CAS Number: 152626-78-3
• Molecular Formula: C8H7BrN2O
• Molecular Weight: 227.058
• MDL Number: MFCD11007880
• SMILES: COc1cc2[nH]ncc2cc1Br

Computed Properties

• Complexity: 167
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.2

Upstream Synthesis Route

The compound 5-Bromo-6-methoxy-1H-indazole serves as a versatile building block in chemical synthesis due to its unique structural features and reactivity. With its bromine substituent at the 5-position and methoxy group at the 6-position on the indazole ring, this compound offers a wide range of synthetic possibilities.In organic synthesis, 5-Bromo-6-methoxy-1H-indazole can be utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. The bromine atom provides a site for further functionalization through various coupling reactions such as Suzuki, Heck, or Stille coupling, enabling the introduction of different functional groups onto the indazole scaffold. The methoxy group, on the other hand, can serve as a directing group in selective functionalization reactions, enhancing regioselectivity and facilitating the synthesis of more complex molecules.Furthermore, the presence of the indazole core in this compound imparts unique bioactivity and pharmacological properties, making it a valuable starting material for the development of novel drug candidates. By leveraging the synthetic utility of 5-Bromo-6-methoxy-1H-indazole, chemists can access a diverse array of structurally diverse compounds with potential applications in medicinal chemistry, material science, and beyond.