398845
醋酸铅（IV）
≥99.99% trace metals basis
别名:
Pb(acac)4, 四乙酸铅
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关于此项目
线性分子式:
Pb(CH3CO2)4
化学文摘社编号:
分子量:
443.38
EC Number:
208-908-0
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
3595640
MDL number:
InChI key
JEHCHYAKAXDFKV-UHFFFAOYSA-J
InChI
1S/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+4/p-4
SMILES string
CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O
assay
≥99.99% trace metals basis
reaction suitability
core: lead, reagent type: catalyst
Application
平稳地诱导向烯烃和炔烃中添加二氟二碘甲烷。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1A - STOT RE 2
存储类别
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
法规信息
新产品
此项目有
Li, A-R. Chen, Q-Y.
Synthesis, 1481-1481 (1997)
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).
[A combined carbohydrate immunocytochemical technic for localization of glycogen in the pancreatic islands of steroid diabetic rats].
R Graf et al.
Acta histochemica. Supplementband, 25, 61-62 (1982-01-01)
G Brückner et al.
Acta histochemica, 74(1), 91-102 (1984-01-01)
Brains obtained from three species of mediterranean cephalopods (Loligo, Sepia, Octopus) were fixed in Bouin's solution. Paraffin sections were cut sequentially at the frontal plane and used for Alcian blue staining (critical electrolyte concentration method), colloidal iron hydroxide staining procedure
Hidehito Urata et al.
Chemical & pharmaceutical bulletin, 56(11), 1611-1612 (2008-11-05)
The first chemical synthesis of two metabolites ((1R,2S,5R,6S)-6-(3,4-dihydroxyphenyl)-2-(3,4-methylenedioxyphenyl)-3,7-dioxabicyclo[3,3,0]octane (SC-1) and (1R,2S,5R,6S)-2,6-bis(3,4-dihydroxyphenyl)-3,7-dioxabicyclo[3,3,0]octane (SC-2)) of sesamin was achieved by a simple two-step approach from sesamin. The approach consists of acetoxylation of the methylenedioxy moiety(ies) with lead(IV) tetraacetate and acid hydrolysis of the
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