1-BOC-4 PIPERIDONE VENDOR | 1-BOC-4 PIPERIDONE BUY

1-BOC-4 PIPERIDONE VENDOR | 1-BOC-4 PIPERIDONE BUY

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Specifications and Properties of 1-n-Boc-4-(Phenylamino)Piperidine Vendor

1-n-Boc-4-(Phenylamino)Piperidine, a compound widely used in organic synthesis, features a molecular structure characterized by a piperidine ring substituted with a phenylamino group and a tert-butoxycarbonyl (Boc) protecting group. With a molecular formula of C15H20N2O2, it has a molecular weight of 256.34 g/mol. The piperidine moiety allows this compound to participate in various chemical reactions, making it a valuable intermediate for medicinal chemistry and drug development.

1-BOC-4 PIPERIDONE VENDOR is a chemical compound used primarily in organic synthesis and pharmaceutical research. It is a derivative of piperidine, a common structural motif in many drugs and bioactive molecules. Below are the properties and specifications of 1-N-BOC-4-(Phenylamino)piperidine, provided for educational and informational purposes only. This compound is typically used in research settings and is not intended for human consumption.

Chemical Specifications

• IUPAC Name: tert-Butyl 4-(phenylamino)piperidine-1-carboxylate
• Chemical Formula: C16H24N2O2
• Molecular Weight: 276.38 g/mol
• Appearance: Typically a white to off-white crystalline powder
• Solubility: Soluble in organic solvents (e.g., ethanol, methanol, dichloromethane); poorly soluble in water
• Melting Point: Approximately 80-85°C (176-185°F)
• Boiling Point: Not well-documented, but likely decomposes before boiling
• Density: Not well-documented

The compound typically exhibits high purity rates, often above 98%, which is crucial for ensuring reproducibility in research applications. Purity can significantly affect the outcome of reactions and the performance of synthesized compounds. Therefore, it is advisable to source 1-n-Boc-4-(Phenylamino)Piperidine from reputable suppliers who provide certificates of analysis to confirm quality. Storage conditions for this chemical should be considered critical; it is recommended to keep the compound in a cool, dry place away from light to maintain its stability and efficacy.

1-n-Boc-4-(Phenylamino)Piperidine Vendor

When handling 1-n-Boc-4-(Phenylamino)Piperidine, safety precautions are paramount. Laboratory personnel should wear appropriate personal protective equipment such as gloves and safety goggles to avoid skin and eye contact. If ingested or if inhalation occurs, follow the standard emergency procedures. Additionally, regulatory considerations must be adhered to; this compound may be subject to regulations regarding its use and distribution due to its potential applications in pharmaceuticals. Checking local guidelines and compliance standards will ensure that researchers and chemists adhere to safe and legal practices when working with 1-n-Boc-4-(Phenylamino)Piperidine.

1-n-Boc-4-(Phenylamino)Piperidine Vendor Names

Other Names:-

Verified
1-BOC-4-(4-BROMO-PHENYLAMINO)-PIPERIDINE
1-Piperidinecarboxylic acid, 4-[(4-bromophenyl)amino]-, 1,1-dimethylethyl ester
2-Methyl-2-propanyl 4-[(4-bromophenyl)amino]-1-piperidinecarboxylate
2-Methyl-2-propanyl-4-[(4-bromphenyl)amino]-1-piperidincarboxylat
4-[(4-Bromophényl)amino]-1-pipéridinecarboxylate de 2-méthyl-2-propanyle
tert-Butyl 4-((4-bromophenyl)amino)piperidine-1-carboxylate

Unverified
1-boc-4-(4-bromophenylamino)-piperidine
1-PIPERIDINECARBOXYLIC ACID, 4-[(4-BROMOPHENYL)AMINO]-,1,1-DIMETHYLETHYL ESTER
4-(4-Bromo-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester
4-(4-Bromophenyl)amino-1-(tert-butoxycarbonyl)piperidine
tert-Butyl 4-(4-bromoanilino)piperidine-1-carboxylate
tert-butyl 4-(4-bromophenylamino)-piperidine-1-carboxylate
tert-butyl 4-[(4-bromophenyl)amino]piperidine-1-carboxylate