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Thermo Scientific Chemicals
(R)-(-)-3-Amino-1-Boc-piperidine, 98%
CAS: 188111-79-7 | C10H20N2O2 | 200.282 g/mol
化学物質識別子
CAS188111-79-7
IUPAC Nametert-butyl 3-aminopiperidine-1-carboxylate
Molecular FormulaC10H20N2O2
InChI KeyAKQXKEBCONUWCL-UHFFFAOYNA-N
SMILESCC(C)(C)OC(=O)N1CCCC(N)C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to yellow
Assay (GC)≥97.5%
FormLiquid
Optical Rotation-27.5 ± 1.5? (neat)
Refractive Index1.4710-1.4750 @ 20?C
(R)-(-)-3-Amino-1-Boc-piperidine is used as an intermediate in the manufacture of various substances such as pharmaceuticals.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(R)-(-)-3-Amino-1-Boc-piperidine is used as an intermediate in the manufacture of various substances such as pharmaceuticals.
Solubility
Immiscible with water.
Notes
Air and moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents and strong acids.
(R)-(-)-3-Amino-1-Boc-piperidine is used as an intermediate in the manufacture of various substances such as pharmaceuticals.
Solubility
Immiscible with water.
Notes
Air and moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only
General References:
- Choi, H. E.; Choi, J. H.; Lee, J. Y.; Kim, J. H.; Kim, J. H.; Lee, J. K.; Kim, G. I.; Park, Y.; Chi, Y. H.; Paik, S. H.; Lee, J. H.; Lee, K. T. Synthesis and evaluation of nicotinamide derivative as anti-angiogenic agents. Bioorg. Med. Chem. Lett. 2013, 23 (7), 2083-2088.
- Wang, J.; Kuryatov, A.; Jin, Z.; Norleans, J.; Kamenecka, T. M.; Kenny, P. J.; Lindstrom, J. A Novel alpha2/alpha4 Subtype-selective Positive Allosteric Modulator of Nicotinic Acetylcholine Receptors Acting from the C-tail of an alpha Subunit. J. Biol. Chem. 2015, 290 (48), 28834-28846.