| Weight | 141.258 g/mol |
|---|---|
| Formula | C9H19N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2,2,6,6-Tetramethylpiperidine (768-66-1)
2,2,6,6-tetramethylpiperidide
Score:
#2061 in Physics
,
#6423 in Chemistry
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- Absolute rate constants for the reactions of some carbon-centered radicals with 2,2,6,6-tetramethylpiperidine-N-oxyl (Journal of Organic Chemistry, 1988)
- A NOVEL SPIN-LABELED AMINO-ACID DERIVATIVE FOR USE IN PEPTIDE-SYNTHESIS - (9-FLUORENYLMETHYLOXYCARBONYL)-2,2,6,6-TETRAMETHYLPIPERIDINE-N-OXYL-4-AMINO-4-CARBOXYLIC ACID (Journal of the American Chemical Society, 1993)
- Aerobic Oxidation of Benzylic Alcohols in Water by 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO)/Copper(II) 2-N-Arylpyrrolecarbaldimino Complexes (Advanced Synthesis & Catalysis, 2009)
- Mechanism of the oxidation of alcohols by 2,2,6,6-tetramethylpiperidine nitrosonium cation (Tetrahedron Letters, 1986)
- Lithium 2,2,6,6-tetramethylpiperidide and related, strong, proton-specific bases. Evaluation in synthesis (Journal of the American Chemical Society, 1973)
- Effects of lithium salts on the stereochemistry of ketone enolization by lithium 2,2,6,6-tetramethylpiperidide (LiTMP). A convenient method for highly E-selective enolate formation (Journal of the American Chemical Society, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,2,6,6-tetramethylpiperidide
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SMILESCC1(CCCC(N1)(C)C)C
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InChIKeyRKMGAJGJIURJSJ-UHFFFAOYSA-N
- Pubchem - 2,2,6,6-Tetramethylpiperidine
- Wikipedia - 2,2,6,6-tetramethylpiperidine
2,2,6,6-Tetramethylpiperidine or TMP or HTMP is an organic compound of the amine class. In appearance, it is a colorless liquid and has a "fishy", amine-like odor. This amine is used in chemistry as a hindered base (hindered amine).
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