Tetrapropylammonium perruthenate structure
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Common Name | Tetrapropylammonium perruthenate | ||
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CAS Number | 114615-82-6 | Molecular Weight | 351.425 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C12H28NO4Ru | Melting Point | 160ºC | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS03, GHS07 |
Signal Word | Danger |
Use of Tetrapropylammonium perruthenateTetrapropylammonium perruthenate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | tetrapropylammonium perruthenate |
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Synonym | More Synonyms |
Description | Tetrapropylammonium perruthenate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Melting Point | 160ºC |
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Molecular Formula | C12H28NO4Ru |
Molecular Weight | 351.425 |
Exact Mass | 352.106232 |
PSA | 74.27000 |
LogP | 2.96800 |
Appearance of Characters | crystal | green |
Storage condition | 2-8°C |
Stability | store cold |
Water Solubility | Insoluble in water. |
Symbol |
GHS03, GHS07 |
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Signal Word | Danger |
Hazard Statements | H272-H315-H319-H335 |
Precautionary Statements | P220-P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
Hazard Codes | O: Oxidizing agent;Xi: Irritant; |
Risk Phrases | R36/37/38;R5;R8 |
Safety Phrases | S17-S26-S36 |
RIDADR | UN 1479 5.1/PG 2 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 5.1 |
HS Code | 2923900090 |
Precursor 0 | |
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DownStream 10 | |
HS Code | 2923900090 |
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Summary | 2923900090 other quaternary ammonium salts and hydroxides。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
Oxidation of hydroxyl-substituted organotrifluoroborates.
J. Am. Chem. Soc. 128 , 9634, (2006) Potassium- and tetra-n-butylammonium organotrifluoroborates containing hydroxyl groups have been prepared and oxidized using several common oxidants. Aryl-, alkenyl-, and alkyltrifluoroborates contain... |
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A double donor-activated ruthenium(VII) catalyst: synthesis of enantiomerically pure THF-diols.
Angew. Chem. Int. Ed. Engl. 49(9) , 1587-90, (2010)
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Single-flask synthesis of N-acylated indoles by catalytic dehydrogenative coupling with primary alcohols.
Org. Lett. 11(7) , 1651-4, (2009) Indoles and alcohols can be coupled in a dehydrogenative process catalyzed by tetrapropylammonium perruthenate. This efficient approach to indolylamides proceeds in a single flask under mild condition... |
MFCD00074914 |
N,N,N-Tripropyl-1-propanaminium oxido(trioxo)ruthenium |
Tetrapropylammonium perruthenate |
N,N,N-Tripropylpropan-1-aminium oxido(trioxo)ruthenium |
TPAP |