103438-85-3 | 4-Fluoro-3-hydroxybenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$14.00	$10.00
250mg	97%	in stock	$23.00	$17.00
1g	97%	in stock	$49.00	$34.00
5g	97%	in stock	$169.00	$118.00
25g	97%	in stock	$634.00	$444.00
100g	97%	in stock	$1,878.00	$1,315.00

Description

• Catalog Number: AD48025
• Chemical Name: 4-Fluoro-3-hydroxybenzaldehyde
• CAS Number: 103438-85-3
• Molecular Formula: C7H5FO2
• Molecular Weight: 140.1118
• MDL Number: MFCD11110190
• SMILES: O=Cc1ccc(c(c1)O)F

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

4-Fluoro-3-hydroxybenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, this compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique chemical properties make it especially valuable in the synthesis of complex organic molecules, allowing for efficient and selective reactions to take place.One key application of 4-Fluoro-3-hydroxybenzaldehyde in chemical synthesis is as a precursor for the synthesis of pharmaceutical compounds. By undergoing specific reactions, this compound can be transformed into more complex structures that possess biological activity, making it an essential intermediate in the pharmaceutical industry. Additionally, its presence in the structure of certain drugs can enhance their efficacy or modify their pharmacokinetic properties.Furthermore, 4-Fluoro-3-hydroxybenzaldehyde can be utilized in the synthesis of agrochemicals, such as pesticides and herbicides. Its structural features can be strategically modified to impart desired properties, enabling the creation of effective and environmentally friendly agricultural products. This compound plays a crucial role in the development of crop protection agents that help increase agricultural productivity and sustainability.In the realm of fine chemicals, 4-Fluoro-3-hydroxybenzaldehyde finds applications in the synthesis of specialty chemicals, fragrances, and flavor compounds. Its ability to participate in diverse chemical transformations allows for the creation of compounds with unique sensory properties or industrial applications. This compound is instrumental in the production of high-value chemicals that contribute to various sectors, including cosmetics, food, and materials science.Overall, 4-Fluoro-3-hydroxybenzaldehyde is a valuable asset in chemical synthesis, serving as a versatile building block for the creation of diverse compounds with potential applications in pharmaceuticals, agrochemicals, and fine chemicals. Its role in the development of new products and technologies highlights its importance in advancing various industries and scientific endeavors.

Literature

• Generalized solvent scales as a tool for investigating solvent dependence of spectroscopic and kinetic parameters. Application to fluorescent BODIPY dyes.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20100730