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Tert-butoxycarbonyl-1,4-diaminobutane

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Identification
Molecular formula
C9H20N2O2
CAS number
30364-44-4
IUPAC name
tert-butyl N-(4-aminobutyl)carbamate
State
State

At room temperature, tert-butyl N-(4-aminobutyl)carbamate is found in a solid state. It is generally handled as a powder.

Melting point (Celsius)
52.50
Melting point (Kelvin)
325.65
Boiling point (Celsius)
251.00
Boiling point (Kelvin)
524.15
General information
Molecular weight
188.27g/mol
Molar mass
188.2740g/mol
Density
0.9604g/cm3
Appearence

The compound tert-butyl N-(4-aminobutyl)carbamate appears as a white solid powder.

Comment on solubility

Solubility of tert-butyl N-(4-aminobutyl)carbamate

The solubility of tert-butyl N-(4-aminobutyl)carbamate (C9H20N2O2) can be influenced by various factors due to its unique chemical structure. Here are some key points regarding its solubility:

  • Polar vs. Non-Polar: The presence of the carbamate functional group contributes to the compound's polar characteristics, enhancing its potential solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability of tert-butyl N-(4-aminobutyl)carbamate to form hydrogen bonds with water molecules facilitates its solubility.
  • Alkyl Chains: The tert-butyl group, being hydrophobic, may limit solubility in extreme polar solvents but can enhance compatibility with organic solvents.
  • Temperature Dependency: Like most compounds, the solubility can increase with temperature, making it more soluble in warm conditions.

In general, one might expect this compound to have moderate solubility in water and better solubility in organic solvents. However, empirical testing is essential to determine precise solubility values in various media.

Interesting facts

Interesting Facts about Tert-butyl N-(4-aminobutyl)carbamate

Tert-butyl N-(4-aminobutyl)carbamate is a fascinating compound that plays a significant role in various areas of chemistry and pharmaceuticals. Here are some key points that highlight its significance:

  • Functional Groups: This compound contains both an amine and a carbamate functional group, which are crucial for its reactivity and interactions in biological systems.
  • Biological Relevance: Tert-butyl N-(4-aminobutyl)carbamate is being studied for its potential as a drug candidate, particularly in the field of medicinal chemistry. It can contribute to the development of therapies targeting various diseases.
  • Versatility: The tert-butyl group provides a unique steric effect that can influence the compound’s stability and reactivity, making it a valuable tool in synthetic organic chemistry.
  • Synthesis and Applications: Due to its structure, this compound may serve as an intermediate in the synthesis of more complex molecules, illustrating the versatility and importance of carbamate derivatives in organic synthesis.

As chemists delve deeper into the properties and potential applications of tert-butyl N-(4-aminobutyl)carbamate, they illuminate pathways for innovation in drug design and chemical synthesis. The intricate interplay of its functional groups allows for a wide array of chemical reactions, making it a hot topic in both academic and industrial research.

In the words of a noted chemist, "The study of compounds like tert-butyl N-(4-aminobutyl)carbamate exemplifies the beauty and complexity of organic chemistry, opening doors to new scientific horizons."

Synonyms
68076-36-8
tert-Butyl N-(4-aminobutyl)carbamate
N-Boc-1,4-butanediamine
tert-Butyl (4-aminobutyl)carbamate
N-Boc-1,4-diaminobutane
tert-butyl 4-aminobutylcarbamate
NH2-C4-NH-Boc
1-Boc-amino-1,4-butanediamine
MFCD00210019
N-(tert-Butoxycarbonyl)-1,4-diaminobutane
Carbamic acid, (4-aminobutyl)-, 1,1-dimethylethyl ester
tert-butyl(4-aminobutyl)carbamate
N-(4-Aminobutyl)carbamic Acid tert-Butyl Ester
N-(4-aminobutyl)carbamic acid t-butyl ester
4-aminobutylcarbamic acid tert-butyl ester
N-(4-Aminobutyl)carbamic Acid 1,1-Dimethylethyl Ester
N-(tert-Butoxycarbonyl)-1,4-butanediamine
H2N(CH2)4NHBoc
N-Boc-butane-1,4-diamine
t-butyl 4-aminobutylcarbamate
SCHEMBL181700
t-butyl 4-amino-butylcarbamate
CHEMBL3356838
4-t-butoxycarbonylamino-butylamine
CS-D0144
BBL101371
STL555167
tert-butyl-N-(4-aminobutyl)carbamate
AKOS005146189
tert-butyl 4-aminobutylaminocarboxylate
AC-2382
FB75329
GS-5840
N-t-butyloxycarbonyl-1,4-diaminobutane
BP-14003
HY-40178
n-tert-butyloxycarbonyl-1,4-diaminobutane
N-tert.-butoxycarbonyl-1,4-diaminobutane
SY003980
1,1-dimethylethyl (4-aminobutyl)carbamate
(4-aminobutyl)-carbamic acid t-butyl ester
DB-030404
(4-amino-butyl)-carbamic acid t-butyl ester
A1373
N-(tert-butoxycarbonyl)-1,4-diamino butane
N-(tert-butoxycarbonyl)-1,4-diamino-butane
(4-amino-butyl)carbamic acid tert-butyl ester
(4-aminobutyl)-carbamic acid tert-butyl ester
N-(4-aminobutyl)-carbamic acid t-butyl ester
(4-Amino-butyl)-carbamic acid tert-butyl ester
EN300-125900
N-Boc-1,4-butanediamine, >=97.0% (GC/NT)
tert-butyl N-(4-aminobutyl)carbamate,hydrochloride
(4-aminobutyl)carbamic acid 1,1-dimethylethyl ester
629-298-6