CAS 1882-42-4

4-(1,1-Dimethylethyl)piperidine

Description:

4-(1,1-Dimethylethyl)piperidine, also known as tert-butylpiperidine, is an organic compound characterized by its piperidine ring substituted with a tert-butyl group at the fourth position. This compound is a colorless to pale yellow liquid with a distinctive amine-like odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic tert-butyl group. The presence of the piperidine ring imparts basic properties to the molecule, allowing it to act as a nucleophile in various chemical reactions. Its structure contributes to its stability and reactivity, making it useful in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, 4-(1,1-Dimethylethyl)piperidine can exhibit unique properties such as enhanced lipophilicity, which can influence its biological activity and interactions in chemical processes. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes and should be used in well-ventilated areas.

Formula: C₉H₁₉N

InChI: InChI=1S/C9H19N/c1-9(2,3)8-4-6-10-7-5-8/h8,10H,4-7H2,1-3H3

InChI key: InChIKey=HAKKTZOUPCDMCN-UHFFFAOYSA-N

SMILES: C(C)(C)(C)C1CCNCC1

Synonyms:

• Piperidine, 4-(1,1-dimethylethyl)-
• NSC 364049
• 4-(1,1-Dimethylethyl)piperidine
• Piperidine, 4-tert-butyl-
• 4-tert-Butylpiperidine

4-tert-butylpiperidine

CAS: 1882-42-4

Formula: C₉H₁₉N

Molecular weight: 141.2539

Ref: IN-DA002GRT

4-tert-Butylpiperidine

CAS: 1882-42-4

4-tert-Butylpiperidine is an organic chemical compound that is a colorless liquid with a strong, unpleasant odor. 4-tert-Butylpiperidine is a nonselective, nucleophilic sulfoxide oxidant that reacts with the electron pair of a sulfur atom in sulfoxides and halides to form alkylating products. It has been used in the oxidation of toluene to benzoic acid and in the synthesis of piperazine. 4-tert-Butylpiperidine can also be used to chlorinate aluminium or as an analytical reagent for the detection of chloride ions. The chemical structure includes two isomeric forms, namely alpha and beta. Alpha is more stable than beta and will react faster; however, beta can be isolated from mixtures of the two compounds by distillation.

Formula: C₉H₁₉N

Purity: Min. 95%

Molecular weight: 141.25 g/mol

Ref: 3D-BAA88242