3011-34-5 | 4-Hydroxy-3-nitrobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$16.00	$11.00
5g	97%	in stock	$19.00	$13.00
10g	97%	in stock	$20.00	$14.00
25g	97%	in stock	$21.00	$15.00
100g	97%	in stock	$53.00	$38.00
500g	97%	in stock	$137.00	$96.00

Description

• Catalog Number: AB67637
• Chemical Name: 4-Hydroxy-3-nitrobenzaldehyde
• CAS Number: 3011-34-5
• Molecular Formula: C7H5NO4
• Molecular Weight: 167.1189
• MDL Number: MFCD00007117
• SMILES: O=Cc1ccc(c(c1)[N+](=O)[O-])O
• NSC Number: 138267

Computed Properties

• Complexity: 188
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.5

Literature

• 3-Chloro-N'-(4-hy-droxy-3-nitro-benzyl-idene)benzohydrazide methanol disolvate.

  Acta crystallographica. Section E, Structure reports online 20110701

• 4-Hy-droxy-N'-(4-hy-droxy-3-nitro-benzyl-idene)benzohydrazide.

  Acta crystallographica. Section E, Structure reports online 20110201

• 2-Hy-droxy-N'-(4-hy-droxy-3-nitro-benzyl-idene)benzohydrazide.

  Acta crystallographica. Section E, Structure reports online 20110201

• Aqabamycins A-G: novel nitro maleimides from a marine Vibrio species: II. Structure elucidation.

  The Journal of antibiotics 20100601

• Aqabamycins A-G: novel nitro maleimides from a marine Vibrio species. I. Taxonomy, fermentation, isolation and biological activities.

  The Journal of antibiotics 20100601

• (E)-3-Bromo-N'-(4-hydr-oxy-3-nitro-benzyl-idene)benzohydrazide.

  Acta crystallographica. Section E, Structure reports online 20090801

• (E)-4-(4-Hydr-oxy-3-nitro-benzyl-idene-amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one.

  Acta crystallographica. Section E, Structure reports online 20081001

• 4-Hydr-oxy-3-nitro-benzaldehyde.

  Acta crystallographica. Section E, Structure reports online 20080501

• Acid-promoted reaction of the stilbene antioxidant resveratrol with nitrite ions: mild phenolic oxidation at the 4'-hydroxystiryl sector triggering nitration, dimerization, and aldehyde-forming routes.

  The Journal of organic chemistry 20060526

• Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives.

  Bioorganic & medicinal chemistry letters 20060201