CAS 1722-95-8
:(R)-(-)-2-METHYLPIPERIDINE
Description:
(R)-(-)-2-Methylpiperidine is a chiral amine with the molecular formula C7H17N. It features a piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, with a methyl group attached to the second carbon atom. This compound is characterized by its distinct stereochemistry, as indicated by the (R)-(-) designation, which refers to its specific spatial arrangement of atoms. It is a colorless to pale yellow liquid at room temperature and has a characteristic amine odor. The compound is soluble in organic solvents and exhibits basic properties due to the presence of the nitrogen atom, which can accept protons. (R)-(-)-2-Methylpiperidine is utilized in various applications, including as a building block in organic synthesis and in the production of pharmaceuticals. Its chiral nature makes it particularly valuable in asymmetric synthesis, where it can influence the stereochemical outcome of reactions. Safety precautions should be observed when handling this compound, as it may cause irritation to the skin and eyes.
Formula:C6H13N
InChI:InChI=1/C6H13N.ClH/c1-6-4-2-3-5-7-6;/h6-7H,2-5H2,1H3;1H/t6-;/m1./s1
SMILES:C[C@@H]1CCCCN1.Cl
Synonyms:- (R)-2-Methyl-Piperidine
- (R)-2-METHYLPIPERIDINE
- (R)-2-Methylpiperidine 95%
- (R)-(-)-2-METHYLPIPERIDINE HCl
- Piperidine, 2-methyl-, (2R)-
- 2-(R)-Methylpiperidine
- Berberine chloride primary reference standard
- (2R)-2-Methylpiperidine
- (R)-2-methylpiperidine hydrochloride
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Found 4 products.
Piperidine, 2-methyl-, (2R)-
CAS:Formula:C6H13NPurity:96%Color and Shape:LiquidMolecular weight:99.1741(R)-2-Methylpiperidine
CAS:(R)-2-MethylpiperidineFormula:C6H13NPurity:97%Color and Shape: colorless liquidMolecular weight:99.17g/mol(R)-2-Methylpiperidine
CAS:<p>(R)-2-Methylpiperidine is a chiral molecule that is an inhibitor of the chemokine receptor 4 (CXCR4). It has been shown to inhibit the growth of glioma cells and is being investigated as a potential cancer treatment. (R)-2-Methylpiperidine binds to the CXCR4 receptor, preventing it from binding with chemokines. This prevents the interaction between chemokines and their receptors, which leads to decreased inflammation in the body. The stereoisomers of this molecule are nonlethal and can be used for research purposes. The enantiopure form is also available for use in pharmaceuticals as a toolbox drug, or as a preparative agent in organic synthesis.</p>Formula:C6H13NPurity:Min. 95%Molecular weight:99.17 g/mol



