578-39-2 | 4-Hydroxy-2-methylbenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$16.00	$11.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$47.00	$33.00

Description

• Catalog Number: AB67614
• Chemical Name: 4-Hydroxy-2-methylbenzoic acid
• CAS Number: 578-39-2
• Molecular Formula: C8H8O3
• Molecular Weight: 152.1473
• MDL Number: MFCD02182261
• SMILES: Oc1ccc(c(c1)C)C(=O)O
• NSC Number: 85496

Computed Properties

• Complexity: 155
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.5

Upstream Synthesis Route

4-Hydroxy-2-methylbenzoic acid, also known as o-cresotic acid, plays a crucial role in chemical synthesis due to its unique structure and properties. This compound is commonly used as a building block in organic chemistry for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 4-Hydroxy-2-methylbenzoic acid is its use as a starting material for the production of salicylic acid derivatives. By reacting o-cresotic acid with different reagents and catalysts, chemists can introduce specific functional groups to the molecule, allowing for the synthesis of a wide range of salicylic acid derivatives with diverse applications in medicine and industry.Additionally, 4-Hydroxy-2-methylbenzoic acid can be converted into ester derivatives through esterification reactions. These esters can serve as valuable intermediates in the synthesis of fragrances, flavors, and other fine chemicals.Furthermore, o-cresotic acid can be utilized in the preparation of liquid crystals, which are essential components in various electronic devices and display technologies. By incorporating this compound into the molecular structure of liquid crystals, researchers can tailor their physical properties and enhance their performance in electronic applications.Overall, the versatile nature of 4-Hydroxy-2-methylbenzoic acid makes it a valuable building block in chemical synthesis, enabling the creation of a wide array of compounds with diverse industrial and scientific applications.

Literature

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  Patient preference and adherence 20120101

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  International journal of molecular sciences 20090401

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  Environmental science and pollution research international 20020101