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tert-butyl N-(5-aminopentyl)carbamate

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Identification
Molecular formula
C10H22N2O2
CAS number
72858-26-3
IUPAC name
tert-butyl N-(5-aminopentyl)carbamate
State
State

At room temperature, tert-butyl N-(5-aminopentyl)carbamate is typically in a liquid state, though it can solidify at lower temperatures. The physical state can vary slightly based on purity and environment.

Melting point (Celsius)
20.00
Melting point (Kelvin)
293.20
Boiling point (Celsius)
269.50
Boiling point (Kelvin)
542.70
General information
Molecular weight
216.32g/mol
Molar mass
216.3240g/mol
Density
0.9688g/cm3
Appearence

The compound tert-butyl N-(5-aminopentyl)carbamate typically appears as a colorless to yellowish liquid or solid, depending on the temperature and environment. It is often used in chemical synthesis and may have a slight characteristic odor.

Comment on solubility

Solubility of tert-butyl N-(5-aminopentyl)carbamate

When considering the solubility of the compound tert-butyl N-(5-aminopentyl)carbamate (C10H22N2O2), a few important factors come into play:

  • Polarity: The presence of both hydrophobic tert-butyl groups and hydrophilic carbamate functionalities suggests a mixed polarity nature.
  • Solvent Compatibility: This compound is likely to exhibit solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), due to its carbon backbone. However, it may have limited solubility in water, primarily due to the bulky tert-butyl group.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, making it more soluble in hot solvents compared to cold.

In general, it can be stated that:

  1. The compound is expected to have moderate solubility in polar organic solvents.
  2. Due to its structural features, it may demonstrate low solubility in water, which is typical for many carbamate derivatives.
  3. Assessing solubility in various solvents can provide valuable insights for practical applications and formulation strategies.

In conclusion, understanding the solubility of tert-butyl N-(5-aminopentyl)carbamate is key to its potential uses, and testing in various mediums will be essential to fully characterize its behavior.

Interesting facts

Interesting Facts about Tert-butyl N-(5-aminopentyl)carbamate

Tert-butyl N-(5-aminopentyl)carbamate is a unique compound that plays a significant role in various fields of chemistry and biology. Here are some fascinating insights:

  • Versatile Applications: This compound is primarily used in organic synthesis and as an intermediate in the preparation of pharmaceutical compounds. Its functional groups make it a valuable asset in designing bioactive molecules.
  • Amine Reactivity: The presence of the amine group in its structure enhances its reactivity, allowing it to participate in various nucleophilic reactions. It can serve as a building block for more complex amine chemistry.
  • Carbamate Formation: Tert-butyl N-(5-aminopentyl)carbamate contains a carbamate moiety, which is known for its stability and low toxicity. These features make it useful in developing safer agrochemicals and pharmaceuticals.
  • Potential in Drug Development: Researchers are exploring its potential in drug development, particularly in creating compounds that modulate biological pathways. Its structural properties can lend themselves to significant pharmacological activities.
  • Environmental Considerations: The synthesis of such compounds often integrates environmentally friendly practices. Chemists focus on reducing waste and utilizing green chemistry principles during its manufacturing, showcasing a commitment to sustainability.

In summary, tert-butyl N-(5-aminopentyl)carbamate represents a bridge between practical chemical applications and innovative research. With ongoing studies and the potential to contribute to advances in chemistry and pharmacology, it remains a compound of interest in scientific exploration.

Synonyms
51644-96-3
N-Boc-cadaverine
N-Boc-1,5-diaminopentane
tert-butyl (5-aminopentyl)carbamate
tert-Butyl N-(5-aminopentyl)carbamate
1-Boc-Amino-1,5-pentanediamine
NH2-C5-NH-Boc
N-(5-Aminoamyl)carbamic Acid tert-Butyl Ester
N-(tert-Butoxycarbonyl)-1,5-diaminopentane
boc-1,5-diaminopentane
MFCD00210020
N-Boc-1,5-pentanediamine
Carbamic acid, (5-aminopentyl)-, 1,1-dimethylethyl ester
tert-butyl 5-aminopentylcarbamate
N-1-Boc-1,5-diaminopentane HCl
N-(5-Aminopentyl)carbamic Acid tert-Butyl Ester
tert-butyl(5-aminopentyl)carbamate
N-1-Boc-1,5-diaminopentane . HCl
N1-Boc-1,5-pentanediamine
N-Boc cadaverine
BocNH(CH2)5NH2
SCHEMBL220281
N-tert-butoxycarbonyl cadaverine
t-butyl(5-aminopentyl)carbamate
DTXSID90274430
BBL103789
STL557599
XH1128
AKOS007930261
5-(tert-butoxycarbonylamino)pentylamine
5-tertbutoxycarbonylamino-1-pentylamine
CS-W004710
HY-W004710
N-Boc-cadaverine, >=97.0% (NT)
N-t-butyloxycarbonyl-1,5-diaminopentane
5-tert-butoxycarbonylamino-1-pentylamine
N-(t-butoxycarbonyl)-1,5-diaminopentane
N-tert-butoxycarbonyl-1,5-diaminopentane
AC-26913
AS-30509
BP-28264
SY057270
N-(tert-Butoxycarbonyl)-1,5-pentanediamine
A1374
A7612
EN300-185974
(5-Amino-pentyl)-carbamic acid tert-butyl ester
5-[(tert.-butyloxycarbonyl)amino]-1-pentylamine
tert-butyl 5-aminopentylcarbamate;N-Boc-cadaverine
629-297-0