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About This Item
Product Name
Triethylphosphine solution, 1.0 M in toluene
InChI key
RXJKFRMDXUJTEX-UHFFFAOYSA-N
SMILES string
CCP(CC)CC
InChI
1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
form
liquid
reaction suitability
reagent type: ligand
reaction type: Arylations
concentration
1.0 M in toluene
density
0.857 g/mL
functional group
phosphine
Quality Level
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Application
- Regioselective formation of alcohols from hydrocarbonylation of alkenes
- Bronsted acid-assisted synthesis of dihydropyrones from aromatic aldehydes and allenoates
- Silaboration of enynes
- Conversion of phenylacetic acids to phenylacetonitriles of benzonitriles
- Thermal decomposition of platinum and palladium naphthalenediyl
- Asymmetrical Morita-Baylis-Hillman reaction
- Regioselective formation of alcohols from hydrocarbonylation of alkenes.
- Bronsted acid-assisted synthesis of dihydropyrones from aromatic aldehydes and allenoates.
- Silaboration of enynes.
- Conversion of phenylacetic acids to phenylacetonitriles of benzonitriles.
- Thermal decomposition of platinum and palladium naphthalenediyl.
- Asymmetrical Morita-Baylis-Hillman reaction.
signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3
target_organs
Central nervous system
Storage Class
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
flash_point_f
44.6 °F
flash_point_c
7 °C
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