3934-87-0 | 3,4-Dihydroxy-5-methoxybenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$11.00	$8.00
1g	95%	in stock	$21.00	$15.00
5g	95%	in stock	$48.00	$34.00
100g	95%	in stock	$955.00	$668.00

Description

• Catalog Number: AB63728
• Chemical Name: 3,4-Dihydroxy-5-methoxybenzaldehyde
• CAS Number: 3934-87-0
• Molecular Formula: C8H8O4
• Molecular Weight: 168.1467
• MDL Number: MFCD00016610
• SMILES: COc1cc(C=O)cc(c1O)O
• NSC Number: 16679

Computed Properties

• Complexity: 159
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: -0.3

Upstream Synthesis Route

3,4-Dihydroxy-5-methoxybenzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules and pharmaceuticals. With its unique structure, $name$ plays a crucial role in the development of new materials and compounds. In chemical synthesis, $name$ is commonly employed as a precursor in the manufacture of specialized dyes, fragrances, and natural products. Its reactivity and functional groups make it a valuable tool for organic chemists seeking to design and produce complex molecules with specific properties. Additionally, $name$ is utilized in the synthesis of bioactive compounds, serving as a critical intermediate in the production of pharmaceuticals and agrochemicals. Its role in chemical synthesis extends to the creation of novel materials with tailored properties, showcasing its significance in advancing the field of organic chemistry.

Literature

• Sequencing around 5-hydroxyconiferyl alcohol-derived units in caffeic acid O-methyltransferase-deficient poplar lignins.

  Plant physiology 20100601

• Impact of linker strain and flexibility in the design of a fragment-based inhibitor.

  Nature chemical biology 20090601