1-N-Boc-4-(Phenylamino)piperidine CAS 125541-22-2

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4-Anilino-1-Boc-piperidine (Item No. 29119) is an analytical reference standard that is structurally similar to known opioids. 4-Anilino-1-Boc-piperidine is a precursor in the synthesis of 4-anilinopiperidine . This product is intended for research and forensic applications.

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1-N-Boc-4-(Phenylamino)piperidine cas 125541-22-2

piperidine CAS 125541-22-2
piperidine CAS 125541-22-2

1-N-Boc-4-(Phenylamino)piperidine product information:

Product Name 1-N-Boc-4-(Phenylamino)piperidine
Synonyms TERT-BUTYL 4-ANILINOTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE;4-(Phenylamino)piperidine, N1-BOC protected;1-N-BOC-4-(PHENYLAMINO)PIPERIDINE;tert-butyl 4-anilinotetrahydro-1(2H)-pyridinecarboxylate (en)
CAS NO 125541-22-2
EINECS 203-105-0
Molecular Formula C16H24N2O2
Molecular Weight 276.37
Melting Point 136-137
Boiling Point 400.6±38.0 °C(Predicted)
Flash Point 196.1±26.8 °C
Density 1.107±0.06 g/cm3(Predicted)
Assay ≥99%
Grade Pharmaceutical Grade
Solubility DMF: 15mg/mL
DMSO: 25mg/mL
Ethanol: 25mg/mL
Ethanol:PBS (pH 7.2) (1:1): 0.5mg/mL
Appearance Pale Brown Solid
Storage Keep away from light, in a cool and dry place, sealed
Usage Intermediate in the preparation of Fentanyl derivatives

1-N-Boc-4-(Phenylamino) piperidine uses

Intermediate in the preparation of Fentanyl derivatives.

The biochemical and physiological effects of Boc-Phe-Pip are not well-understood. However, it is known that Boc-Phe-Pip is a strong base, and its reaction with acids can result in the formation of a variety of products. These products can then be used in a variety of applications, including the synthesis of peptides and proteins, organic synthesis, and drug development.

The synthesis of Boc-Phe-Pip is typically carried out using a two-step process. The first step involves the reaction of piperidine with 4-bromobenzaldehyde in the presence of a base, such as sodium hydroxide. This reaction yields the desired product, 4-bromophenylpiperidine. The second step involves the reaction of 4-bromophenylpiperidine with Boc-anhydride in the presence of a base, such as sodium hydroxide, to yield the desired product, Boc-Phe-Pip.

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