CAS 158406-99-6: (S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate

Description: (S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The bromomethyl group introduces a reactive site, allowing for further chemical modifications or reactions, such as nucleophilic substitutions. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals due to its potential biological activity. The carboxylate functional group contributes to its reactivity and can participate in various chemical reactions, including esterification and amidation. Additionally, the stereochemistry indicated by the (S) configuration suggests that the compound exhibits chirality, which can influence its biological interactions and pharmacological properties. Overall, this compound is notable for its structural features that facilitate diverse applications in synthetic organic chemistry.

Synonyms:

• tert-butyl (3S)-3-(bromomethyl)piperidine-1-carboxylate

1-Piperidinecarboxylic acid, 3-(bromomethyl)-, 1,1-dimethylethyl ester, (3S)-

CAS: 158406-99-6

• Formula: C₁₁H₂₀BrNO₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 278.186

(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate

CAS: 158406-99-6

• Purity: 95%
• Molecular weight: 278.19g/mol

(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate

CAS: 158406-99-6

• Purity: 95.0%
• Color and Shape: Liquid, No data available.
• Molecular weight: 278.19000244140625

(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate

CAS: 158406-99-6

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• Formula: C₁₁H₂₀BrNO₂
• Purity: Min. 95%
• Molecular weight: 278.19 g/mol