2144-08-3 | 2,3,4-Trihydroxybenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$14.00	$10.00
25g	98%	in stock	$15.00	$11.00
100g	98%	in stock	$53.00	$38.00

Description

• Catalog Number: AB54152
• Chemical Name: 2,3,4-Trihydroxybenzaldehyde
• CAS Number: 2144-08-3
• Molecular Formula: C7H6O4
• Molecular Weight: 154.12014
• MDL Number: MFCD00003325
• SMILES: O=Cc1ccc(c(c1O)O)O
• NSC Number: 22595

Computed Properties

• Complexity: 147
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 0.9

Literature

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  Evidence-based complementary and alternative medicine : eCAM 20110101

• Label free inhibitor screening of hepatitis C virus (HCV) NS5B viral protein using RNA oligonucleotide.

  Sensors (Basel, Switzerland) 20110101

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  Journal of medicinal chemistry 20101111

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  Acta crystallographica. Section E, Structure reports online 20101101

• The severity of Puumala hantavirus induced nephropathia epidemica can be better evaluated using plasma interleukin-6 than C-reactive protein determinations.

  BMC infectious diseases 20100101

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

  Nature chemical biology 20090601

• 2,3,4-Trihydroxy-benzaldehyde.

  Acta crystallographica. Section E, Structure reports online 20080801

• Pyrogallol and its analogs can antagonize bacterial quorum sensing in Vibrio harveyi.

  Bioorganic & medicinal chemistry letters 20080301

• Carbohydrazones of substituted salicylaldehydes as potential lead compounds for the development of narrow-spectrum antimicrobials.

  Zeitschrift fur Naturforschung. C, Journal of biosciences 20070101

• Self-activating nuclease activity of copper (II) complexes of hydroxyl-rich ligands.

  Journal of inorganic biochemistry 20060101

• alpha-Glucosidase inhibition of 6-hydroxyflavones. Part 3: Synthesis and evaluation of 2,3,4-trihydroxybenzoyl-containing flavonoid analogs and 6-aminoflavones as alpha-glucosidase inhibitors.

  Bioorganic & medicinal chemistry 20050301

• New non-nucleoside inhibitors of hepatitis C virus RNA-dependent RNA polymerase.

  Biochemistry. Biokhimiia 20040701

• Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.

  Journal of food protection 20031001