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CAS RN: 546-67-8 | Product Number: L0021
Lead Tetraacetate (contains Acetic Acid)
Purity: >96.0%(T)
Synonyms:
- LTA (contains Acetic Acid)
- Lead(IV) Acetate (contains Acetic Acid)
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
25G |
£46.00
|
Contact Us | Contact Us |
|
500G |
£389.00
|
Contact Us | Contact Us |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | L0021 |
Purity / Analysis Method | >96.0%(T) |
Molecular Formula / Molecular Weight | C__8H__1__2O__8Pb = 443.38 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Moisture Sensitive,Heat Sensitive |
CAS RN | 546-67-8 |
Reaxys Registry Number | 3595640 |
PubChem Substance ID | 87571991 |
Merck Index (14) | 5423 |
MDL Number | MFCD00008693 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(Iodometric Titration) | min. 96.0 % |
NMR | confirm to structure |
Properties (reference)
Melting Point | 180 °C |
Solubility (soluble in) | Nitrobenzene, Benzene, Chloroform, Alcohol |
GHS
Pictogram | |
Signal Word | Danger |
Hazard Statements | H302 + H332 : Harmful if swallowed or if inhaled. H315 : Causes skin irritation. H373 : May cause damage to organs through prolonged or repeated exposure. H341 : Suspected of causing genetic defects. H350 : May cause cancer. H360Df : May damage the unborn child. Suspected of damaging fertility. H410 : Very toxic to aquatic life with long lasting effects. H272 : May intensify fire; oxidizer. |
Precautionary Statements | P273 : Avoid release to the environment. P260 : Do not breathe dust. P220 : Keep away from clothing and other combustible materials. P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P201 : Obtain special instructions before use. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P391 : Collect spillage. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. |
Related Laws:
EC Number | 208-908-0 |
RTECS# | AI5300000 |
Transport Information:
UN Number | UN3087 |
Class | 5.1 / 6.1 |
Packing Group | III |
HS Number | 2915290000 |
Application
Generation of Benzyne using Pb(OAc)4 and Synthesis of Dibenzocyclobutadiene
Reference
- Reactivity of Dehydrometallophthalocyanines and -porphyrazines
Application
Oxidation of 1,2-Diols (Criegee Oxidation)1)
Typical Procedure:
To a solution of olefine 1 (11.9 mg, 0.030 mmol) and DMAP (7.33 mg, 0.060 mmol, 2 eq.) in t-BuOH (100 µL) is added a solution of OsO4 (7.62 mg, 0.030 mmol, 1 eq.) in water (200 µL). The orange-red solution is stirred at rt for 5-10 min. Solid Na2SO3 (19 mg, 0.15 mmol, 5 eq.) is added. The resulting mixture is applied directly to preparative TLC (CHCl3 : MeOH : NH4OH = 25 : 10 : 1) and diol is collected by washing silica gel with a mixture of CHCl3 : MeOH = 2 : 1. Concentration under reduced pressure (< 25 ℃) affords the slightly unstable diol 2, which is dissolved in CH2Cl2 (2 mL). The solution then is cooled to -20 ℃ and AcOH (9.0 mg, 8.6 µL, 5 eq.) is added, followed by solid Pb(OAc)4 (11 mg, 0.025 mmol) in portions. TLC (CH2Cl2 : MeOH = 1 : 1 and 25 : 1) monitors the end of the reaction. The resulting yellow solution is stirred at -20 ℃ for 5-10 min, washed with water, saturated NaHCO3 and brine, dried over Na2SO4 and evaporated under reduced pressure to give 3 (8.5 mg, Y. 71%) of silica gel labile ketone as a yellow powder.
To a solution of olefine 1 (11.9 mg, 0.030 mmol) and DMAP (7.33 mg, 0.060 mmol, 2 eq.) in t-BuOH (100 µL) is added a solution of OsO4 (7.62 mg, 0.030 mmol, 1 eq.) in water (200 µL). The orange-red solution is stirred at rt for 5-10 min. Solid Na2SO3 (19 mg, 0.15 mmol, 5 eq.) is added. The resulting mixture is applied directly to preparative TLC (CHCl3 : MeOH : NH4OH = 25 : 10 : 1) and diol is collected by washing silica gel with a mixture of CHCl3 : MeOH = 2 : 1. Concentration under reduced pressure (< 25 ℃) affords the slightly unstable diol 2, which is dissolved in CH2Cl2 (2 mL). The solution then is cooled to -20 ℃ and AcOH (9.0 mg, 8.6 µL, 5 eq.) is added, followed by solid Pb(OAc)4 (11 mg, 0.025 mmol) in portions. TLC (CH2Cl2 : MeOH = 1 : 1 and 25 : 1) monitors the end of the reaction. The resulting yellow solution is stirred at -20 ℃ for 5-10 min, washed with water, saturated NaHCO3 and brine, dried over Na2SO4 and evaporated under reduced pressure to give 3 (8.5 mg, Y. 71%) of silica gel labile ketone as a yellow powder.
References
- 1)Eine oxydative spaltung von glykolen (II. Mitteil. über oxydationen mit blei(IV)-salzen)
- 2)Enantioselective total synthesis of aspidophytine
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