41833-13-0 | 4-Hydroxy-3-nitrobenzyl alcohol

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$16.00	$11.00
1g	98%	in stock	$23.00	$16.00
10g	98%	in stock	$30.00	$21.00
15g	98%	in stock	$32.00	$23.00
25g	98%	in stock	$37.00	$26.00

Description

• Catalog Number: AF70436
• Chemical Name: 4-Hydroxy-3-nitrobenzyl alcohol
• CAS Number: 41833-13-0
• Molecular Formula: C7H7NO4
• Molecular Weight: 169.1348
• MDL Number: MFCD00024249
• SMILES: OCc1ccc(c(c1)[N+](=O)[O-])O

Computed Properties

• Complexity: 167
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

4-Hydroxy-3-nitrobenzyl alcohol is a key intermediate in chemical synthesis processes, especially in the field of organic chemistry. This compound serves as a versatile building block for creating various functional molecules due to its unique chemical properties.In chemical synthesis, 4-Hydroxy-3-nitrobenzyl alcohol can be utilized as a precursor in the production of pharmaceutical compounds, agrochemicals, and other fine chemicals. Its reactive hydroxyl and nitro functional groups make it an important starting material for synthesizing complex organic compounds through various chemical transformations.One common application of 4-Hydroxy-3-nitrobenzyl alcohol is in the synthesis of photoactive compounds, such as photoresists and photoinitiators. The presence of the hydroxyl group allows for the attachment of photoactive moieties, while the nitro group can participate in redox reactions, making it useful in photochemical processes.Additionally, 4-Hydroxy-3-nitrobenzyl alcohol can also be employed in the preparation of advanced materials like polymers, dyes, and specialty chemicals. Its ability to undergo selective chemical modifications enables chemists to tailor the properties of the final products for specific applications in materials science and other related fields.Overall, the versatility and reactivity of 4-Hydroxy-3-nitrobenzyl alcohol make it a valuable tool in chemical synthesis, offering researchers and chemists a wide range of possibilities for creating novel compounds with diverse functionalities and applications.

Literature

• 18F-FEAnGA for PET of β-glucuronidase activity in neuroinflammation.

  Journal of nuclear medicine : official publication, Society of Nuclear Medicine 20120301

• Synthesis and biological activity of the prodrug of class I major histocompatibility peptide GILGFVFTL activated by beta-glucuronidase.

  Journal of medicinal chemistry 20020214