5769-33-5 | 4-Bromo-2,6-dimethylbenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$7.00	$5.00
250mg	97%	in stock	$15.00	$11.00
1g	97%	in stock	$38.00	$27.00
5g	97%	in stock	$57.00	$40.00
25g	97%	in stock	$199.00	$139.00
100g	97%	in stock	$654.00	$458.00

Description

• Catalog Number: AG78577
• Chemical Name: 4-Bromo-2,6-dimethylbenzaldehyde
• CAS Number: 5769-33-5
• Molecular Formula: C9H9BrO
• Molecular Weight: 213.0712
• MDL Number: MFCD11227151
• SMILES: O=Cc1c(C)cc(cc1C)Br

Computed Properties

• Complexity: 135
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.8

Upstream Synthesis Route

The compound 4-Bromo-2,6-dimethylbenzaldehyde plays a crucial role in chemical synthesis due to its unique properties and reactivity. This compound is commonly utilized as a building block in the preparation of various organic compounds. It serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.One of the key applications of 4-Bromo-2,6-dimethylbenzaldehyde is its use as a starting material for the synthesis of biologically active molecules. Its aldehyde functional group allows for further functionalization through various chemical reactions, such as nucleophilic addition and condensation reactions. This enables chemists to introduce specific functional groups or structural motifs into the target molecules with precision.Moreover, 4-Bromo-2,6-dimethylbenzaldehyde can participate in cross-coupling reactions, such as Suzuki coupling or Heck reaction, to form carbon-carbon bonds. These reactions are widely employed in the synthesis of complex organic compounds, including natural products and materials. The bromine substituent in the benzaldehyde moiety can also serve as a directing group in metal-catalyzed transformations, facilitating regioselective bond formations.Overall, the strategic placement of bromine and methyl groups in the benzaldehyde scaffold makes 4-Bromo-2,6-dimethylbenzaldehyde a valuable building block for designing and synthesizing diverse organic compounds with tailored functionalities and properties. Its utility in chemical synthesis highlights its significance in the development of new materials and pharmaceuticals.