22446-37-3 | (2-Hydroxy-phenyl)-acetic acid methyl ester

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$12.00	$9.00
5g	98%	in stock	$15.00	$10.00
10g	98%	in stock	$19.00	$14.00
25g	98%	in stock	$36.00	$26.00

Description

• Catalog Number: AB49526
• Chemical Name: (2-Hydroxy-phenyl)-acetic acid methyl ester
• CAS Number: 22446-37-3
• Molecular Formula: C9H10O3
• Molecular Weight: 166.1739
• MDL Number: MFCD00090077
• SMILES: COC(=O)Cc1ccccc1O

Computed Properties

• Complexity: 156
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.2

Upstream Synthesis Route

2-Hydroxy-benzeneacetic acid methyl ester, commonly known as aspirin, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the pharmaceutical industry, where it is utilized in the production of various medications. Aspirin is a key ingredient in many pain relievers and anti-inflammatory drugs due to its ability to inhibit the production of prostaglandins, which are responsible for mediating pain and inflammation in the body.In addition to its pharmaceutical applications, 2-Hydroxy-benzeneacetic acid methyl ester is also utilized in organic chemistry as a building block for the synthesis of other compounds. Its ester functionality allows for easy manipulation of the molecule, making it a valuable intermediate in the preparation of various organic compounds. Furthermore, aspirin can be used as a catalyst in certain chemical reactions, facilitating the formation of desired products.Overall, the application of 2-Hydroxy-benzeneacetic acid methyl ester in chemical synthesis is widespread and essential in both the pharmaceutical and organic chemistry fields. Its versatility and reactivity make it a valuable compound for the creation of a diverse range of products.

Literature

• Synthesis, characterization and structure-activity relationship analysis of novel depsides as potential antibacterials.

  European journal of medicinal chemistry 20090401