1026089-09-7 | 2-(4-Bromo-2-methoxyphenyl)acetic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$7.00	$5.00
1g	97%	in stock	$18.00	$12.00
5g	97%	in stock	$29.00	$21.00
10g	97%	in stock	$50.00	$35.00
25g	97%	in stock	$119.00	$84.00

Description

• Catalog Number: AA10031
• Chemical Name: 2-(4-Bromo-2-methoxyphenyl)acetic acid
• CAS Number: 1026089-09-7
• Molecular Formula: C9H9BrO3
• Molecular Weight: 245.07
• MDL Number: MFCD11847505
• SMILES: COc1cc(Br)ccc1CC(=O)O

Computed Properties

• Complexity: 184
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2

Upstream Synthesis Route

2-(4-Bromo-2-methoxyphenyl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block for a variety of organic transformations. This compound plays a crucial role in the preparation of pharmaceuticals, agrochemicals, and advanced materials due to its unique chemical properties and reactivity.In chemical synthesis, $name$ serves as a valuable starting material for the formation of complex molecules through various synthetic pathways. Its functional groups enable the introduction of different substituents and modifications, making it an essential tool for the construction of diverse molecular structures. Additionally, the presence of the bromine and methoxy groups offers opportunities for further derivatization and functionalization to tailor the compound for specific applications.Moreover, the carboxylic acid functionality in 2-(4-Bromo-2-methoxyphenyl)acetic acid allows for facile conversion to various derivative compounds, expanding its utility in the synthesis of specialty chemicals and intermediates. This compound can undergo reactions such as esterification, amidation, and other transformations to yield products with enhanced properties and functionalities.Through its strategic placement in synthetic routes, 2-(4-Bromo-2-methoxyphenyl)acetic acid contributes to the efficient and strategic assembly of complex molecular architectures. Its versatility and reactivity make it an indispensable tool for organic chemists and researchers involved in drug discovery, material science, and chemical manufacturing.