1206-55-9 | 3,6-Dimethoxy-2-nitrobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$50.00	$35.00
1g	97%	in stock	$118.00	$83.00
5g	97%	in stock	$510.00	$357.00
25g	97%	in stock	$2,044.00	$1,431.00

Description

• Catalog Number: AD33497
• Chemical Name: 3,6-Dimethoxy-2-nitrobenzaldehyde
• CAS Number: 1206-55-9
• Molecular Formula: C9H9NO5
• Molecular Weight: 211.1715
• MDL Number: MFCD00091893
• SMILES: COc1ccc(c(c1[N+](=O)[O-])C=O)OC
• NSC Number: 107746

Computed Properties

• Complexity: 239
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• XLogP3: 1.2

Upstream Synthesis Route

3,6-Dimethoxy-2-nitrobenzaldehyde, also known by its chemical formula C9H9NO5, plays a crucial role in chemical synthesis due to its versatile reactivity and unique chemical properties.1. Oxidation Reactions: 3,6-Dimethoxy-2-nitrobenzaldehyde can serve as a key building block in the synthesis of various organic compounds through oxidation reactions. For example, it can be used as a precursor in the synthesis of different types of nitroalkenes or nitroalcohols when subjected to appropriate reagents and conditions.2. Nitroalkene Synthesis: By utilizing 3,6-Dimethoxy-2-nitrobenzaldehyde in chemical reactions, researchers can access nitroalkenes, which are valuable intermediates in the preparation of diverse organic molecules such as pharmaceuticals, agrochemicals, and materials.3. Nitro-Michael Addition: Another significant application of 3,6-Dimethoxy-2-nitrobenzaldehyde is in the Nitro-Michael addition reaction, where the aldehyde functionality enables the addition of a nitrogen-containing nucleophile. This reaction is widely used in the construction of complex molecules with high stereochemical control.In summary, the strategic placement of functional groups in 3,6-Dimethoxy-2-nitrobenzaldehyde makes it a versatile starting material for various synthetic transformations, allowing chemists to access a wide array of structurally diverse organic compounds for different applications.

Literature

• Studies on quinones. Part 37. Synthesis and biological activity of o-aminoester functionalised benzo- and naphtho[2,3-b]thiophenequinones.

  Chemical & pharmaceutical bulletin 20020901