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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
Regulatory Information
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Li, A-R. Chen, Q-Y.
Synthesis, 1481-1481 (1997)
Luis Moreno-Osorio et al.
Magnetic resonance in chemistry : MRC, 45(11), 993-996 (2007-09-19)
Two naturally occurring 11-nordrimanes were synthesized, and their (1)H and (13)C NMR spectra were unambiguously assigned in full for the first time.
H Mallesha et al.
Nucleosides, nucleotides & nucleic acids, 21(4-5), 385-392 (2002-08-17)
Lead tetraacetate (LTA) oxidation of alpha-Phenyl-N-(4-bipheny])nitrone (8) to give a new ultimate carcinogen, N-acetoxy-N-benzoyl-4-aminobiphenyl (9) which was reacted with deoxyguanosine (dG) at pH 6.9 to give nucleoside derivative, N-(benzoyl)-N-(deoxyguanosin-8-yl)-4-aminobiphenyl (10). Following debenzoylation with sodium carbonate-methanol leads to N-(2'-deoxyguanosin-8-yl)-4-aminobiphenyl (11).


