179701
Triethylborane solution
1.0 M in THF
Sinónimos:
Triethylboron
About This Item
Productos recomendados
form
liquid
reaction suitability
reagent type: reductant
concentration
1.0 M in THF
density
0.865 g/mL at 25 °C
SMILES string
CCB(CC)CC
InChI
1S/C6H15B/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI key
LALRXNPLTWZJIJ-UHFFFAOYSA-N
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Application
- Allylation of aldehydes
- Decarboxylative C-C bond cleavage reactions
- Rhenium hydride / boron Lewis acid cocatalysis of alkene hydrogenations
- Regioselective hydroxyalkylation of unsaturated oxime ethers
Reactant for radical reductions of alkyl bromides with N-heterocyclic carbene boranes
Reactant for synthesis of tetramethylammonium trialkylphenylborate salts with oxidation potential
- Allylation of aldehydes
- Decarboxylative C-C bond cleavage reactions
- Rhenium hydride / boron Lewis acid cocatalysis of alkene hydrogenations
- Regioselective hydroxyalkylation of unsaturated oxime ethers
It can be employed as a reactant for radical reductions of alkyl bromides with N-heterocyclic carbene boranes and for the synthesis of tetramethylammonium trialkylphenylborate salts.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Skin Corr. 1A - STOT SE 3 - Water-react 2
target_organs
Central nervous system, Respiratory system
supp_hazards
Storage Class
4.2 - Pyrophoric and self-heating hazardous materials
wgk_germany
WGK 1
flash_point_f
1.4 °F - closed cup
flash_point_c
-17 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Artículos
We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.
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