94569-84-3 | 2-Bromo-5-fluorobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$6.00	$4.00
5g	97%	in stock	$8.00	$5.00
10g	97%	in stock	$9.00	$6.00
25g	97%	in stock	$15.00	$10.00
100g	97%	in stock	$46.00	$32.00
500g	97%	in stock	$160.00	$112.00

Description

• Catalog Number: AB43857
• Chemical Name: 2-Bromo-5-fluorobenzaldehyde
• CAS Number: 94569-84-3
• Molecular Formula: C7H4BrFO
• Molecular Weight: 203.0085
• MDL Number: MFCD00142872
• SMILES: O=Cc1cc(F)ccc1Br

Computed Properties

• Complexity: 129
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.2

Upstream Synthesis Route

2-Bromo-5-fluorobenzaldehyde, also known as $name$, is a versatile compound frequently utilized in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound is valued for its unique structural properties, which enable it to participate in a variety of important reactions in organic synthesis.In chemical synthesis, $name$ serves as a crucial intermediate in the production of diverse compounds due to its reactivity and ability to undergo a range of transformations. Its precise manipulation allows chemists to introduce specific functional groups or modify existing ones, leading to the synthesis of complex molecules with desired characteristics.One prominent application of 2-Bromo-5-fluorobenzaldehyde is its role as a valuable precursor in the preparation of biologically active compounds or pharmacologically relevant molecules. By leveraging the reactivity of $name$, chemists can access important chemical bonds and structural motifs necessary for the development of new drugs or therapeutic agents.Moreover, the versatility of 2-Bromo-5-fluorobenzaldehyde extends beyond medicinal chemistry, finding utility in the synthesis of agrochemicals and specialty chemicals as well. Its ability to serve as a key synthetic intermediate in the construction of diverse chemical entities underscores its significance in modern synthetic organic chemistry.Overall, the strategic incorporation of 2-Bromo-5-fluorobenzaldehyde in chemical synthesis enables chemists to access a wide array of functionalized compounds with potential applications across various industries. Its importance as a building block underscores its value in the pursuit of novel chemical entities with beneficial properties.

Literature

• 5-Fluoro-1,3-dihydro-2,1-benzoxaborol-1-ol.

  Acta crystallographica. Section E, Structure reports online 20110201

• Vibrational spectra, ab initio/DFT electronic structure calculations, and normal coordinate analysis of 2-bromo-5-fluorobenzaldehyde.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20091201

• Ethyl 4-(2-bromo-5-fluoro-phen-yl)-6-methyl-1-phenyl-2-thioxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20080801