Weight | 87.166 g/mol |
---|---|
Formula | C5H13N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Neopentylamine (5813-64-9)
2,2-dimethyl-1-propylamine
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- Lanthanide complexes derived from (R)-1,1-binaphthyl-2,2-bis(neopentylamine){Li(THF)4}{Ln[(R)-C20H12N2(C10H22)]2}(Ln = Sm, Yb) novel catalysts for enantioselective intramolecular hydroamination (Chemical Communications, 2003)
- The Enantioselective Synthesis of Neopentylamine Derivatives (Synlett, 1995)
- Studies in stereochemistry. XL. Unusual magnitudes of optical rotations of imines of neopentylamine-1-d and ethylamine-1-d (Journal of the American Chemical Society, 1969)
- Lanthanide complexes derived from (R)-1,1?-binaphthyl-2,2?-bis(neopentylamine) ? {Li(THF)4}{Ln[(R)-C20H12N2(C10H22)]2} (Ln = Sm, Yb) ? novel catalysts for enantioselective intramolecular hydroaminationElectronic supplementary information (ESI) available: full characterisation. See http://www.rsc.org/suppdata/cc/b3/b310954b/ (Chemical Communications, 2003)
- Thermodynamics of intermediate ionmolecule complexes or kinetics of competing reactions? The reactions of low-energy isobutylamine and neopentylamine molecular ions (Journal of The Chemical Society-perkin Transactions 1, 1986)
- Deamination of optically active neopentylamine-1-d (Journal of the American Chemical Society, 1967)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,2-dimethyl-1-propylamine
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SMILESCC(C)(C)CN
-
InChIKeyXDIAMRVROCPPBK-UHFFFAOYSA-N
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