1186422-15-0 | 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	2 weeks	$331.00	$232.00
500mg	97%	2 weeks	$448.00	$314.00
1g	97%	2 weeks	$604.00	$423.00
5g	97%	2 weeks	$2,011.00	$1,408.00

Description

• Catalog Number: AI11980
• Chemical Name: 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole
• CAS Number: 1186422-15-0
• Molecular Formula: C14H19BN2O3
• Molecular Weight: 274.12325999999996
• MDL Number: MFCD18384162
• SMILES: COc1ccc(c2c1[nH]nc2)B1OC(C(O1)(C)C)(C)C

Upstream Synthesis Route

7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole is a versatile compound widely utilized in modern chemical synthesis processes. With its unique structure and reactive properties, this compound serves as a valuable building block in the creation of various organic molecules.One key application of 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole is its role in Suzuki-Miyaura coupling reactions. This compound functions as an essential boron-containing reagent in these coupling reactions, enabling the formation of carbon-carbon bonds under mild conditions. By incorporating 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole into these synthetic pathways, chemists can efficiently construct complex organic structures with high precision and efficiency.Moreover, the presence of the methoxy group in 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole enhances its nucleophilic properties, making it a suitable candidate for various nucleophilic substitution reactions. This reactivity broadens the scope of synthetic transformations that can be achieved using this compound, further highlighting its significance in chemical synthesis.In essence, 7-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole plays a crucial role in the construction of complex organic molecules through Suzuki-Miyaura coupling and other synthetic pathways. Its versatility and reactivity make it a valuable tool for chemists seeking to design and synthesize novel compounds for a diverse range of applications in the field of organic chemistry.