10502-44-0 | 4-Methoxymandelic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$15.00	$10.00
1g	98%	in stock	$19.00	$13.00
10g	98%	in stock	$32.00	$23.00
25g	98%	in stock	$40.00	$28.00

Description

• Catalog Number: AE08082
• Chemical Name: 4-Methoxymandelic acid
• CAS Number: 10502-44-0
• Molecular Formula: C9H10O4
• Molecular Weight: 182.1733
• MDL Number: MFCD00004233
• SMILES: COC1=CC=C(C=C1)C(C(=O)O)O

Computed Properties

• Complexity: 173
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.6

Upstream Synthesis Route

2-Hydroxy-2-(4-methoxyphenyl)acetic acid, also known as veratric acid, serves as a valuable building block in chemical synthesis due to its versatile reactivity and unique structural features. In organic chemistry, veratric acid is commonly used as a starting material for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its hydroxyl and carboxylic acid functional groups make it a sought-after intermediate for the production of complex molecules.One notable application of 2-Hydroxy-2-(4-methoxyphenyl)acetic acid is its utilization in the synthesis of natural products and bioactive compounds. By selectively modifying the functional groups of veratric acid, chemists can access a wide range of derivatives with different properties and applications in medicine and biotechnology.Furthermore, veratric acid can be employed in the development of new materials such as polymers and sensors, showcasing its significance beyond traditional organic synthesis. Its ability to undergo various chemical transformations makes it a valuable tool for researchers in the field of materials science and chemical engineering.Overall, the application of 2-Hydroxy-2-(4-methoxyphenyl)acetic acid in chemical synthesis extends to diverse areas of research and industry, offering endless possibilities for innovation and discovery.

Literature

• alpha-Ketocarboxylic acid-based inhibitors of protein tyrosine phosphatases.

  Bioorganic & medicinal chemistry letters 20010723