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Phenylpropyl carbamate

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Identification
Molecular formula
C10H13NO2
CAS number
101-38-2
IUPAC name
3-phenylpropyl carbamate
State
State

At room temperature, 3-Phenylpropyl carbamate is in a solid state.

Melting point (Celsius)
48.50
Melting point (Kelvin)
321.65
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
179.22g/mol
Molar mass
179.2180g/mol
Density
1.0925g/cm3
Appearence

3-Phenylpropyl carbamate is a crystalline solid with a white to off-white appearance.

Comment on solubility

Solubility of 3-phenylpropyl carbamate (C10H13NO2)

The solubility of 3-phenylpropyl carbamate is influenced by both its molecular structure and the interactions it can establish with solvents. As an organic compound, it often exhibits interesting solubility characteristics:

  • Polar solvents: 3-phenylpropyl carbamate is likely to have moderate solubility in polar solvents such as water due to its carbamate functional group, which allows for hydrogen bonding.
  • Non-polar solvents: It may demonstrate better solubility in non-polar organic solvents, owing to the hydrophobic phenyl group that can engage in London dispersion forces.
  • Temperature effects: Generally, an increase in temperature can enhance the solubility of organic compounds, so elevated temperatures may favor the dissolution of 3-phenylpropyl carbamate.

As with many organic compounds, the specific conditions—such as pH, temperature, and solvent composition—can significantly affect its solubility profile. In practical applications, it is essential to consider these factors when predicting and testing the solubility of 3-phenylpropyl carbamate in various environments.

Interesting facts

Interesting Facts about 3-Phenylpropyl Carbamate

3-Phenylpropyl carbamate is a fascinating chemical compound with notable applications and properties. Here are some intriguing aspects of this compound:

  • Structure and Composition: The compound features a propyl chain with a phenyl group, making it an interesting study in terms of steric effects and electronic interactions within its structure.
  • Biological Activity: As a carbamate, this compound can exhibit biological activity, particularly in areas such as neurotransmitter modulation. It has potential applications in the development of pharmaceuticals and agrochemicals.
  • Synthesis: The synthesis of 3-phenylpropyl carbamate typically involves the reaction of phenylpropylamine with a carbonyl compound, showcasing interesting organic synthesis techniques.
  • Research Potential: Due to its functional groups, 3-phenylpropyl carbamate can serve as a crucial building block in the design of more complex molecules, motivating ongoing research into its derivatives.
  • Safety Considerations: Like many carbamates, safety precautions are essential when handling this compound, as it can exhibit toxicity under certain conditions, similar to other members of its chemical class.

The exploration of 3-phenylpropyl carbamate provides insight into the intricate relationship between chemical structure and biological function, making it a valuable compound for further scientific investigation.

Synonyms
phenprobamate
3-Phenylpropyl carbamate
673-31-4
Spantol
Proformiphen
Ansepron
Actiphan
Actozine
Fenprobamato
Qumamquil
Eirenal
Extacol
Nelaxan
Palmita
Tranquil
Benzenepropanol, carbamate
3-Phenyl-1-propanol carbamate
Carbamic acid, 3-phenylpropyl ester
1-Carbamoyloxy-3-phenylpropane
Phenprobamatum
Benzenepropanol carbamate
HG 532
MH 532
gamma-Phenylpropyl carbamate
Fenprobamato [INN-Spanish]
Phenprobamatum [INN-Latin]
1-Propanol, 3-phenyl-, carbamate
MH-532
NSC 44682
NSC 50538
Phenoprobamate
Gamaquil
gamma-Phenylpropylcarbamat
gamma-Phenylpropylcarbamat [German]
Phenprobamate [INN:BAN:DCF:JAN]
EINECS 211-606-1
UJZ473TPS0
NSC 64270
NSC-44682
NSC-50538
NSC-64270
Spantol (TN)
BRN 1959273
DTXSID2046464
PHENPROBAMATE [MI]
PHENPROBAMATE [INN]
PHENPROBAMATE [JAN]
PHENPROBAMATE [MART.]
.gamma.-Phenylpropyl carbamate
MLS001075792
PHENPROBAMATE [WHO-DD]
DTXCID0026464
NSC44682
NSC50538
NSC64270
1-Propanol, carbamate
NCGC00164589-01
SMR000466378
WLN: ZVO3R
.gamma.-Phenylpropylcarbamat
Fenprobamato (INN-Spanish)
Phenprobamatum (INN-Latin)
PHENPROBAMATE (MART.)
MH532
CAS-673-31-4
UNII-UJZ473TPS0
Phenprobamat
Quamaquil
carbamic acid 3-phenylpropyl ester
MFCD00868163
3-phenylpropylcarbamate
Phenprobamate (JAN/INN)
cid_4770
NCIOpen2_000174
MLS000759511
MLS001075579
MLS001075598
MLS001424080
SCHEMBL134496
CHEMBL1079576
BDBM66801
CHEBI:31992
M03BA01
Benzenepropanol, carbamate (9CI)
Phenprobamate - Bio-X trade mark
HMS2051J03
HMS2235C09
HMS3369F14
HMS3393J03
HMS3715H22
Tox21_112215
AKOS006273141
Tox21_112215_1
CCG-100915
DB13354
KS-5236
NC00165
NCGC00164589-02
AC-32475
BP166013
DA-76811
NS00003087
C76122
D01824
Q7181402
BRD-K22009844-001-09-1
BRD-K22009844-001-12-5
211-606-1