lead tetraacetate structure
|
Common Name | lead tetraacetate | ||
|---|---|---|---|---|
| CAS Number | 546-67-8 | Molecular Weight | 443.376 | |
| Density | 2.22 | Boiling Point | 118.1ºC | |
| Molecular Formula | C8H12O8Pb | Melting Point | 175-180ºC | |
| MSDS | Chinese USA | Flash Point | 40ºC | |
| Symbol |
GHS07, GHS08, GHS09 |
Signal Word | Danger | |
| Name | lead tetraacetate |
|---|---|
| Synonym | More Synonyms |
| Density | 2.22 |
|---|---|
| Boiling Point | 118.1ºC |
| Melting Point | 175-180ºC |
| Molecular Formula | C8H12O8Pb |
| Molecular Weight | 443.376 |
| Flash Point | 40ºC |
| Exact Mass | 444.029816 |
| PSA | 105.20000 |
| InChIKey | NVTAREBLATURGT-UHFFFAOYSA-J |
| SMILES | CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Pb] |
| Stability | Stable. Moisture sensitive. Incompatible with water, most metals. |
| Water Solubility | Decomposition |
CHEMICAL IDENTIFICATION
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| Symbol |
GHS07, GHS08, GHS09 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H302 + H332-H360Df-H373-H410 |
| Precautionary Statements | P201-P260-P280-P301 + P312 + P330-P308 + P313 |
| Hazard Codes | T:Toxic;N:Dangerousfortheenvironment; |
| Risk Phrases | R20/22;R33;R50/53;R61;R62 |
| Safety Phrases | S45-S53-S60-S61 |
| RIDADR | UN 2923 |
| WGK Germany | 3 |
| RTECS | AI5300000 |
| Packaging Group | III |
| Hazard Class | 6.1 |
| HS Code | 2915299090 |
| Precursor 7 | |
|---|---|
| DownStream 9 | |
| HS Code | 2915299090 |
|---|---|
| Summary | 2915299090 salts of acetic acid。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:50.0% |
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Chlorodecarboxylation of 17 beta-acetoxy-3-methoxy-9-oxo-9, 11-secoestra-1, 3, 5 (10)-trien-11-oic acid with lead tetraacetate and trityl chloride.
Steroids 39(5) , 537-45, (1982)
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Formation of an unusual dimeric compound by lead tetraacetate oxidation of a corynanthe-type indole alkaloid, mitragynine.
Chem. Pharm. Bull. 50(7) , 960-3, (2002) Lead tetraacetate oxidation of a Corynanthe-type indole alkaloid, mitragynine, produced mainly 7-acetoxyindolenine derivative (2) together with a dimeric compound (4) as a minor product. The novel str... |
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An efficient synthesis of 4 beta- and 6 alpha-hydroxylated bile acids.
Steroids 58(2) , 52-8, (1993) An efficient method for the preparation of 4 beta- and 6 alpha-hydroxylated bile acids has been developed. It involved a highly stereoselective acetoxylation at the 4 beta and 6 alpha positions of 3- ... |
| Lead ethanoate |
| lead,tetraacetate |
| Lead(4+) tetraacetate |
| plumbane, tetrakis(acetyloxy)- |
| EINECS 208-908-0 |
| Plumbic acetate |
| Lead Tetraacetate |
| MFCD00008693 |
| Lead acetate, basic |
| Lead tetracetate |
| Tetraacetoxyplumbane |