추천 제품
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
- 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.
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
One-Step Synthesis of Methyl Arylacetates from Acetophenones Using Lead (IV) Acetate.
Synthesis, 1981(02), 126-127 (1981)
Lead (IV) Acetate.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2005)
A new method for Halodecarboxylation of Acids using Lead (IV) acetate.
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.
Synthesis, 1982(06), 456-457 (1982)
The reaction of 2-(trialkylsiloxy) furans with lead (IV) acetate. The synthesis of dl-pyrenophorin.
Bulletin of the Chemical Society of Japan, 53(4), 1061-1064 (1980)
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