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(3-carbamoyloxy-2-phenyl-propyl) carbamate

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Identification
Molecular formula
C11H14N2O4
CAS number
123456-78-9
IUPAC name
(3-carbamoyloxy-2-phenyl-propyl) carbamate
State
State

This compound is a solid at room temperature. Its melting point suggests it remains solid under standard conditions, contributing to its stable consistency.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.15
Boiling point (Celsius)
423.50
Boiling point (Kelvin)
696.70
General information
Molecular weight
222.26g/mol
Molar mass
222.2570g/mol
Density
1.2680g/cm3
Appearence

The compound (3-carbamoyloxy-2-phenyl-propyl) carbamate appears as a white crystalline solid. It is characterized by its solid state at room temperature, resulting in a crystalline texture that is typical of many organic compounds with aromatic groups.

Comment on solubility

Solubility of (3-carbamoyloxy-2-phenyl-propyl) carbamate

The solubility of the compound (3-carbamoyloxy-2-phenyl-propyl) carbamate, with the chemical formula C11H14N2O4, can be influenced by various factors such as temperature, pH, and the presence of other solutes.

Factors Affecting Solubility

  • Polarity: The presence of functional groups such as carbamoyl and ether can enhance solubility in polar solvents.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds can increase its solubility in water.
  • Temperature: Typically, an increase in temperature can lead to higher solubility for many organic compounds.

Interestingly, solubility is often expressed in terms of specific solvent interactions. It is important to note:

  • The compound may exhibit improved solubility in organic solvents like methanol or ethanol.
  • Water solubility could be moderate, depending on the pH level and stabilizing interactions.

As a rule of thumb, "like dissolves like," so exploring the solvent characteristics in relation to (3-carbamoyloxy-2-phenyl-propyl) carbamate is critical.

Overall, understanding the solubility profile of this compound is vital for its application in pharmaceuticals and chemical synthesis. This knowledge aids in determining effective formulation strategies and can influence bioavailability in drug development.

Interesting facts

Interesting Facts about (3-Carbamoyloxy-2-phenyl-propyl) Carbamate

(3-Carbamoyloxy-2-phenyl-propyl) carbamate is a compound that sparks interest not only due to its unique structure but also its potential applications in various fields. As a member of the carbamate family, it showcases fascinating chemical properties worth exploring.

Key Features:

  • Functional Versatility: This compound contains both a carbamate and a carbamoyloxy functional group, making it a versatile intermediate in organic synthesis.
  • Pharmaceutical Potential: Carbamates, including this one, are often investigated for their potential as pharmaceuticals, including pain relief agents and anti-inflammatory drugs.
  • Biological Activity: Some derivatives exhibit activity against various biological targets, offering a promising avenue for drug discovery and development.
  • Structure Activity Relationship (SAR): The unique substitution pattern can influence its reactivity and biological efficacy, which can be studied through SAR analyses.

Due to the presence of a phenyl group, this compound may also exhibit interesting electronic characteristics, which can enhance its reactivity and interaction with biological molecules. In research settings, it can serve as a model compound for studying the behavior of similar structures and their pathways in medicinal chemistry.

As a hobby or study topic, diving into the world of carbamates can expose students and scientists alike to the importance of functional groups in organic chemistry, showcasing just how subtle changes can create vastly different compounds with unique properties and applications. In the words of a renowned chemist, “Every small atom carries the universe within it,” further emphasizing the significance of compounds such as (3-carbamoyloxy-2-phenyl-propyl) carbamate in unraveling the mysteries of chemistry.

Synonyms
felbamate
25451-15-4
Felbatol
2-Phenylpropane-1,3-diyl dicarbamate
2-Phenyl-1,3-propanediol dicarbamate
Felbamato
Felbamyl
Taloxa
Felbamatum
W-554
1,3-Propanediol, 2-phenyl-, dicarbamate
Felbamatum [Latin]
ADD-03055
carbamic acid 2-phenyltrimethylene ester
W 554
CHEBI:4995
Carbamic acid, 2-phenyltrimethylene ester
EINECS 247-001-4
UNII-X72RBB02N8
NSC-759866
BRN 3345236
X72RBB02N8
DTXSID9023041
HSDB 7525
(3-carbamoyloxy-1,1,3,3-tetradeuterio-2-phenylpropyl) carbamate
MFCD00865296
3-(carbamoyloxy)-2-phenylpropyl carbamate
2-Phenyl-1,3-propanediol 1,3-dicarbamate
MLS000028465
DTXCID903041
4-06-00-05993 (Beilstein Handbook Reference)
Carbamic acid 3-carbamoyloxy-2-phenyl-propyl ester
Felbamatum (Latin)
NSC 759866
NCGC00015429-08
W-554;ADD-03055
Felbamato [Spanish]
SMR000058448
FELBAMATE (MART.)
FELBAMATE [MART.]
FELBAMATE (USP-RS)
FELBAMATE [USP-RS]
Felbamate [USAN:INN]
(3-carbamoyloxy-2-phenylpropyl) carbamate
FELBAMATE (USP MONOGRAPH)
FELBAMATE [USP MONOGRAPH]
Felbatol (TN)
CAS-25451-15-4
SR-01000000089
Felbamate?
ADD 03055
2 Phenyl 1,3 propanediol dicarbamate
Felbamate (Standard)
Felbamate (USPINN)
Tocris-0869
FELBAMATE [INN]
FELBAMATE [MI]
FELBAMATE [HSDB]
FELBAMATE [USAN]
Opera_ID_1738
Prestwick0_000919
FELBAMATE [VANDF]
Lopac-F-0778
Biomol-NT_000203
F 0778
FELBAMATE [WHO-DD]
CHEMBL1094
Lopac0_000524
SCHEMBL34947
MLS001077299
BIDD:GT0463
BPBio1_001258
GTPL5473
FELBAMATE [ORANGE BOOK]
HY-B0184R
EX-A591
N03AX10
HMS2093P19
HMS2234H06
HMS3261J09
HMS3266L12
HMS3370I06
HMS3411P21
HMS3657I11
HMS3675P21
HMS3715D20
HMS3884E11
Pharmakon1600-01505600
BCP27941
HY-B0184
Tox21_110145
Tox21_302368
Tox21_500524
BDBM50088430
NSC759866
s1330
AKOS015895100
Tox21_110145_1
AC-8197
CCG-204614
CS-2068
DB00949
KS-1171
LP00524
SDCCGSBI-0050507.P003
NCGC00015429-01
NCGC00015429-02
NCGC00015429-03
NCGC00015429-04
NCGC00015429-05
NCGC00015429-06
NCGC00015429-07
NCGC00015429-09
NCGC00015429-10
NCGC00015429-11
NCGC00015429-14
NCGC00015429-24
NCGC00023092-02
NCGC00023092-04
NCGC00023092-05
NCGC00023092-06
NCGC00255275-01
NCGC00261209-01
SBI-0050507.P002
DB-046702
AE2 - Newer Anti-epileptic drug mixtures 2
EU-0100524
NS00010360
SW197633-2
(3-aminocarbonyloxy-2-phenyl-propyl) carbamate
C07501
D00536
EN300-119542
AB00382985-18
AB00382985_19
A817858
Q421301
carbamic acid (3-carbamoyloxy-2-phenylpropyl) ester
SR-01000000089-2
SR-01000000089-4
SR-01000000089-7
BRD-K99107520-001-01-9
BRD-K99107520-001-09-2
BRD-K99107520-001-18-3
BRD-K99107520-001-23-3
BRD-K99107520-001-24-1
BRD-K99107520-001-25-8
Z1521554005
Felbamate, United States Pharmacopeia (USP) Reference Standard
247-001-4