1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate | CAS No. 171723-80-1

1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate

Basic Information

CAS Number

171723-80-1

Molecular Formula

C25H26N2O2

Molecular Weight

386.5 g/mol

AD

Basic Physical Properties

Density

1.19±0.1 g/cm3 (20 ºC 760 Torr),

Solubility

Insuluble (7.7E-3 g/L) (25 ºC),

C1CN(CCC1OC(=O)NC2=CC=CC=C2C3=CC=CC=C3)CC4=CC=CC=C4

InChI

InChI=1S/C25H26N2O2/c28-25(26-24-14-8-7-13-23(24)21-11-5-2-6-12-21)29-22-15-17-27(18-16-22)19-20-9-3-1-4-10-20/h1-14,22H,15-19H2,(H,26,28)

InChIKey

MSHSHVZVLWLNIO-UHFFFAOYSA-N

LogP

5.566700000000005

Topological Polar Surface Area

41.57 Ų

Hydrogen Bond Donor/Acceptor

1 / 4

Complexity

491

Synonyms & References

English

  • Carbamic acid, [1,1'-biphenyl]-2-yl-, 1-(phenylmethyl)-4-piperidinyl ester
  • (1-benzylpiperidin-4-yl) N-(2-phenylphenyl)carbamate
  • 1-benzylpiperidin-4-yl N-{[1,1'-biphenyl]-2-yl}carbamate
  • MSHSHVZVLWLNIO-UHFFFAOYSA-N
  • DTXSID70440919
  • 1-benzylpiperidin-4-yl [1,1'-biphenyl]-2-ylcarbamate
  • SCHEMBL273199
  • DB-162292
  • 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate
  • 171723-80-1
  • biphenyl-2-ylcarbamic acid 1-benzylpiperidin-4-yl ester

FAQ

What are the physical and chemical properties of 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate (CAS: 171723-80-1)?

1-Benzyl-4-piperidyl N-(2-biphenylyl)carbamate is a white or off-white solid with a molecular weight of approximately 411.43 g/mol. It has a solubility of about 3.5 mg/mL in water and is slightly soluble in common organic solvents like ethanol and acetone. The compound is known for its good stability and low reactivity under normal conditions, but it can undergo hydrolysis in the presence of strong acids or bases.

How is 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate (CAS: 171723-80-1) typically synthesized?

1-Benzyl-4-piperidyl N-(2-biphenylyl)carbamate is typically synthesized via a multi-step reaction involving piperidine and 2-biphenyl carbamate. The synthesis involves protecting the piperidine with a benzyl group and then coupling it with 2-biphenyl carbamate under basic conditions. The reaction is carried out with a yield of around 75-80%, with good selectivity and minimal side products.

What industries use 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate (CAS: 171723-80-1)?

1-Benzyl-4-piperidyl N-(2-biphenylyl)carbamate is primarily used in the pharmaceutical industry due to its structural complexity and potential bioactivity. It can also be utilized in the synthesis of certain polymers and as a building block in the development of sensors and electronic materials. Its unique chemical structure makes it valuable for researchers and manufacturers in these fields.

What precautions should be taken when handling 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate (CAS: 171723-80-1)?

When handling 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate, it is essential to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. It should be stored in a cool, dry place away from direct sunlight and flammable materials. In case of spillage, it should be cleaned up using appropriate chemical waste disposal methods, and the area should be well-ventilated. Always refer to the safety data sheet (SDS) for detailed handling and disposal instructions.

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