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About This Item
Linear Formula:
Pb(CH3CO2)4
CAS Number:
Molecular Weight:
443.38
EC Number:
208-908-0
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
3595640
MDL number:
assay
≥99.99% trace metals basis
reaction suitability
core: lead, reagent type: catalyst
SMILES string
CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O
InChI
1S/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+4/p-4
InChI key
JEHCHYAKAXDFKV-UHFFFAOYSA-J
Application
Smoothly induces the addition of difluorodiiodomethane to alkenes and alkynes.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1A - STOT RE 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Li, A-R. Chen, Q-Y.
Synthesis, 1481-1481 (1997)
N S Kumar et al.
Carbohydrate research, 291, 109-114 (1996-09-23)
Oxidative decarboxylation of peracetylated welan gum (S-130) with lead tetraacetate resulted in selective cleavage of the glucuronosidic linkages. Products of the degradation were reduced with sodium borohydride, O-deacetylated, and fractionated. Polymeric and oligomeric fractions were separated and analysed by 1H
B H Jennings et al.
Steroids, 37(1), 7-22 (1981-01-01)
A comparative study was made of the reactions of 5-bromo-3 beta, 6 beta-dihydroxy-5 alpha-androstan-17-one 3-acetate (1) with lead tetraacetate alone and in the presence of iodine in both high intensity visible light and in total darkness using a variety of


