1001203-26-4 | 6-methoxy-1-benzothiophene-2-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$54.00	$38.00
250mg	98%	in stock	$95.00	$67.00
1g	98%	in stock	$254.00	$178.00
5g	98%	in stock	$885.00	$620.00

Description

• Catalog Number: AE32586
• Chemical Name: 6-methoxy-1-benzothiophene-2-carbaldehyde
• CAS Number: 1001203-26-4
• Molecular Formula: C10H8O2S
• Molecular Weight: 192.23432
• MDL Number: MFCD11101038
• SMILES: COc1ccc2c(c1)sc(c2)C=O

Upstream Synthesis Route

6-Methoxy-benzo[b]thiophene-2-carbaldehyde, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, this compound is widely used in various organic reactions to introduce functional groups and create diverse chemical structures.One key application of 6-Methoxy-benzo[b]thiophene-2-carbaldehyde is in the synthesis of heterocyclic compounds. Due to its aromatic nature and sulfur-containing heterocycle, this compound serves as an essential precursor in the construction of complex molecules such as pharmaceuticals, agrochemicals, and materials. By participating in condensation, cyclization, and substitution reactions, it enables the formation of new carbon-carbon and carbon-heteroatom bonds, expanding the possibilities for chemical design and synthesis.Furthermore, the presence of the aldehyde functional group in 6-Methoxy-benzo[b]thiophene-2-carbaldehyde offers opportunities for further modifications through various organic transformations. This aldehyde group can participate in reductive amination, nucleophilic addition, and other types of reactions, allowing chemists to tailor the compound for specific applications and synthetic pathways.Overall, 6-Methoxy-benzo[b]thiophene-2-carbaldehyde is a valuable and versatile compound in chemical synthesis, serving as a key intermediate in the creation of diverse organic molecules with unique properties and functions. Its role in building complex structures and enabling functional group manipulations makes it an essential tool for synthetic chemists across different research fields.