| Weight | 188.076 g/mol |
|---|---|
| Formula | C9H21BO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
TRIISOPROPYL BORATE (5419-55-6)
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- Synthesis of boron-doped double-walled carbon nanotubes by the catalytic decomposition of tetrahydrofuran and triisopropyl borate (Carbon, 2011)
- Atomic layer deposition of B-doped ZnO using triisopropyl borate as the boron precursor and comparison with Al-doped ZnO (Journal of Materials Chemistry C, 2015)
- Synthesis of Spiroborate Esters from 1,2-Aminoalcohols, Ethylene Glycol and Triisopropyl Borate: Preparation of (S)-1-(1,3,2-Dioxaborolan-2-yloxy)-3-Methyl-1,1-Diphenylbutan-2-Amine (Organic Syntheses, 2011)
- Triisopropyl borate mediated N-sulfinyl imine formation (Tetrahedron Letters, 2016)
- An improved method for the synthesis of triisopropyl borate ester (Chemical Reagents, 2004)
- Incorporation of Boron Atoms on Graphene Grown by Chemical Vapor Deposition Using Triisopropyl Borate as a Single Precursor (Journal of Nanomaterials, 2017)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESB(OC(C)C)(OC(C)C)OC(C)C
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InChIKeyNHDIQVFFNDKAQU-UHFFFAOYSA-N
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TRIISOPROPYL BORATE
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