546-67-8 | Lead tetraacetate; 5-10% of acetic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$26.00	$18.00
5g	95%	in stock	$27.00	$19.00
10g	95%	in stock	$44.00	$31.00
25g	95%	in stock	$52.00	$36.00
100g	95%	in stock	$139.00	$97.00
500g	95%	in stock	$558.00	$391.00

Description

• Catalog Number: AB48942
• Chemical Name: Lead tetraacetate; 5-10% of acetic acid
• CAS Number: 546-67-8
• Molecular Formula: C8H12O8Pb
• Molecular Weight: 443.3761
• MDL Number: MFCD00008693
• SMILES: [O-]C(=O)C.[O-]C(=O)C.[O-]C(=O)C.[O-]C(=O)C.[Pb+2]

Computed Properties

• Complexity: 25.5
• Covalently-Bonded Unit Count: 5
• Formal Charge: -4
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 8

Literature

• A Drosophila model for toxicogenomics: Genetic variation in susceptibility to heavy metal exposure.

  PLoS genetics 20170701

• Coordinated waves of gene expression during neuronal differentiation of embryonic stem cells as basis for novel approaches to developmental neurotoxicity testing.

  Cell death and differentiation 20110301

• Scope and mechanism of intramolecular aziridination of cyclopent-3-enyl-methylamines to 1-azatricyclo[2.2.1.0(2,6)]heptanes with lead tetraacetate.

  Journal of the American Chemical Society 20090826

• First chemical synthesis of antioxidative metabolites of sesamin.

  Chemical & pharmaceutical bulletin 20081101

• Cyclopentanes from N-amino-glyconolactams. A synthesis of mannostatin A.

  Chemical communications (Cambridge, England) 20030421

• Formation of an unusual dimeric compound by lead tetraacetate oxidation of a corynanthe-type indole alkaloid, mitragynine.

  Chemical & pharmaceutical bulletin 20020701

• Synthesis and characterization of nucleoside derivatives, n-(benzoyl)-n-(deoxyguanosin-8-yl)4-aminobiphenyl and n-(2'-deoxyguanosin-8-yl)4-aminobiphenyl via alpha-phenyl-n-(4-biphenyl)nitrone.

  Nucleosides, nucleotides & nucleic acids 20020101