84194-36-5 | 2-Chloro-4-fluorobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$13.00	$9.00

Description

• Catalog Number: AB43938
• Chemical Name: 2-Chloro-4-fluorobenzaldehyde
• CAS Number: 84194-36-5
• Molecular Formula: C7H4ClFO
• Molecular Weight: 158.5575
• MDL Number: MFCD00042527
• SMILES: O=Cc1ccc(cc1Cl)F

Computed Properties

• Complexity: 129
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.1

Upstream Synthesis Route

2-Chloro-4-fluorobenzaldehyde, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized in the pharmaceutical and agrochemical industries for the synthesis of various biologically active molecules. With its unique structure and reactivity, 2-Chloro-4-fluorobenzaldehyde serves as a key intermediate in the production of a wide range of products.In organic synthesis, 2-Chloro-4-fluorobenzaldehyde can undergo diverse chemical transformations to introduce functional groups and create complex molecular structures. Its electron-withdrawing chloro and fluoro substituents make it a valuable reactant for the synthesis of heterocyclic compounds, such as benzimidazoles and indoles. Additionally, the aldehyde group in 2-Chloro-4-fluorobenzaldehyde enables it to participate in various reactions, including nucleophilic addition and condensation processes.Furthermore, 2-Chloro-4-fluorobenzaldehyde's compatibility with a wide range of reagents and catalysts allows chemists to access novel compounds with tailored properties. By strategically incorporating this compound into synthetic pathways, researchers can expedite the development of new drugs, crop protection agents, and advanced materials. Overall, the strategic use of 2-Chloro-4-fluorobenzaldehyde in chemical synthesis enables the efficient production of valuable molecules with diverse applications.

Literature

• Trimethyl 5-(2-chloro-4-fluoro-phen-yl)-2-phenyl-pyrrolidine-2,3,4-tricarboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20091101