CAS 35661-58-6

Piperidine, 1-(9H-fluoren-9-ylmethyl)-

Description:

Piperidine, 1-(9H-fluoren-9-ylmethyl)-, is an organic compound characterized by its piperidine ring, which is a six-membered saturated heterocycle containing one nitrogen atom. The presence of the 9H-fluoren-9-ylmethyl group indicates that the piperidine nitrogen is substituted with a fluorenylmethyl moiety, contributing to its unique properties. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the reactivity of both the piperidine and fluorenyl groups. The compound may exhibit basic properties due to the nitrogen atom in the piperidine ring, allowing it to participate in various chemical reactions, including nucleophilic substitutions and cyclizations. Safety data should be consulted, as with all chemical substances, to understand its handling, storage, and potential hazards.

Formula: C₁₉H₂₁N

1-((9H-fluoren-9-yl)methyl)piperidine

CAS: 35661-58-6

Formula: C₁₉H₂₁N

Purity: 95%

Color and Shape: Solid

Molecular weight: 263.384

Ref: 10-F495679

1-(9H-Fluoren-9-ylmethyl)piperidine

CAS: 35661-58-6

Formula: C₁₉H₂₁N

Purity: 97%

Color and Shape: Solid

Molecular weight: 263.3767

Ref: IN-DA0037KI

1-((9H-Fluoren-9-yl)methyl)piperidine

CAS: 35661-58-6

1-((9H-Fluoren-9-yl)methyl)piperidine

Purity: 97%

Molecular weight: 263.384g/mol

Ref: 54-OR73704

1-(9-Fluorenylmethyl)piperidine

CAS: 35661-58-6

Formula: C₁₉H₂₁N

Molecular weight: 263.38

Ref: 4Z-P-147106

1-(9-Fluorenylmethyl)piperidine

CAS: 35661-58-6

Applications 1-(9-Fluorenylmethyl)piperidine is an intermediate when synthesizing 9-​Fluorenylmethoxycarbonyl group (FMOC), which is a new amino-protecting group.
References Carpino, L., et al.: J. Org. Chem., 37, 3404 (1972)

Formula: C₁₀H₁₅NO₆S

Color and Shape: Neat

Molecular weight: 277.294

Ref: TR-F532445