| Weight | 97.998 g/mol |
|---|---|
| Formula | C6H15B |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Triethylborane (97-94-9)
Score:
#1151 in Physics
,
#3285 in Chemistry
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- Pd-Catalyzed C3-Selective Allylation of Indoles with Allyl Alcohols Promoted by Triethylborane (Journal of the American Chemical Society, 2005)
- Triethylborane-induced hydrodehalogenation of organic halides by tin hydrides (Bulletin of the Chemical Society of Japan, 1989)
- Powerful solvent effect of water in radical reaction: Triethylborane-induced atom-transfer radical cyclization in water (Journal of the American Chemical Society, 2000)
- Triethylborane-induced stereoselective radical addition of perfluoroalkyl iodides to acetylenes (Tetrahedron Letters, 1989)
- Triethylborane-Initiated Room Temperature Radical Addition of Hypophosphites to Olefins: Synthesis of Monosubstituted Phosphinic Acids and Esters (Journal of Organic Chemistry, 2001)
- An improved radical chain procedure for the deoxygenation of secondary and primary alcohols using diphenylsilane as hydrogen atom donor and triethylborane-air as initiator (Tetrahedron Letters, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 -
SMILESB(CC)(CC)CC
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- Pubchem - Triethylborane
- Wikipedia - triethylborane
Triethylborane (TEB), also called triethylboron, is an organoborane (a compound with a B-C bond). It is a colorless pyrophoric liquid. Its chemical formula is (C2H5)3B, abbreviated Et3B.
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Triethylborane
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