Home Other Building Blocks Lead tetraacetate; 5-10% of acetic acid

Lead tetraacetate; 5-10% of acetic acid

CAS No.:
546-67-8
Catalog Number:
AG00372U
Molecular Formula:
C8H12O8Pb--
Molecular Weight:
443.3761
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
96%
In Stock USA
United States
$13
- +
5g
96%
In Stock USA
United States
$19
- +
25g
96%
In Stock USA
United States
$45
- +
100g
96%
In Stock USA
United States
$100
- +
500g
96%
In Stock USA
United States
$400
- +
Product Description
Catalog Number:
AG00372U
Chemical Name:
Lead tetraacetate; 5-10% of acetic acid
CAS Number:
546-67-8
Molecular Formula:
C8H12O8Pb--
Molecular Weight:
443.3761
MDL Number:
MFCD00008693
IUPAC Name:
lead;tetraacetate
InChI:
InChI=1S/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/p-4
InChI Key:
NVTAREBLATURGT-UHFFFAOYSA-J
SMILES:
[O-]C(=O)C.[O-]C(=O)C.[O-]C(=O)C.[O-]C(=O)C.[Pb+2]
EC Number:
208-908-0
UN Number:
2291
Properties
Complexity:
25.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
5  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
444.03g/mol
Formal Charge:
-4  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
443.376g/mol
Monoisotopic Mass:
444.03g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
161A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
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
Properties