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Merck
모든 사진(1)

주요 문서

185191

Sigma-Aldrich

Lead(IV) acetate

reagent grade, 95%

동의어(들):

Lead tetraacetate, Pb(acac)4

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About This Item

Linear Formula:
Pb(CH3CO2)4
CAS Number:
Molecular Weight:
443.38
Beilstein:
3595640
EC Number:
MDL number:
UNSPSC 코드:
12352302
eCl@ss:
38140424
PubChem Substance ID:
분석:
95%
Grade:
reagent grade
양식:
crystalline powder
powder, crystals or chunks

Grade

reagent grade

Quality Level

분석

95%

양식

crystalline powder
powder, crystals or chunks

반응 적합성

reagent type: catalyst
core: lead

저장 온도

2-8°C

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

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일반 설명

Lead(IV) acetate is an inorganic lead salt. It participates in α-acetoxylation of ketones and oxidative decarboxylation of carboxylic acids. It along with an ionic halide (particularly chloride) salt participates in the decarboxylation of acids to afford alkyl chlorides. It affords the corresponding α,β-unsaturated γ-acetoxy-γ-lactones via reaction with 2-(trimethylsiloxy)furans.

애플리케이션

Lead(IV) acetate (LTA) may be used as an oxidizing reagent for the oxidation of following compounds:
  • unsaturated and aromatic hydrocarbons
  • monohydroxylic and saturated alcohols
  • nitrogen-containing compounds
It may be used for the following conversions:
  • Aromatic primary amines to symmetrical azo compounds.
  • Aliphatic primary amines to alkyl cyanides.
  • Primary amides to carbamates.
  • Hydrazones to azoacetates.
  • 2-(Trimethylsiloxy) furans to α,β-unsaturated γ-acetoxy-γ-lactones.
  • Aryl ethyl ketones to alkyl 2-arylpropanoates.
  • Acetophenones to methyl aryl acetates.
Smoothly induces the addition of difluorodiiodomethane to alkenes and alkynes.

픽토그램

Health hazardExclamation markEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1A - STOT RE 2

Storage Class Code

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


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문서 라이브러리 방문

One-Step Synthesis of Methyl Arylacetates from Acetophenones Using Lead (IV) Acetate.
Myrboh B, et al.
Synthesis, 1981(02), 126-127 (1981)
Lead (IV) Acetate.
Mihailovic ML, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2005)
A new method for Halodecarboxylation of Acids using Lead (IV) acetate.
Kochi JK.
Journal of the American Chemical Society, 87(11), 2500-2502 (1965)
Facile synthesis of alkyl 2-arylpropanoates from aryl ethyl ketones using lead (IV) acetate.
Fujii K, et al.
Synthesis, 1982(06), 456-457 (1982)
The reaction of 2-(trialkylsiloxy) furans with lead (IV) acetate. The synthesis of dl-pyrenophorin.
Asaoka M, et al.
Bulletin of the Chemical Society of Japan, 53(4), 1061-1064 (1980)

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