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Identification
Molecular formula
C19H26N2O6
CAS number
7347-33-5
IUPAC name
[1-(butoxymethyl)-2-(5-ethyl-2,4,6-trioxo-5-phenyl-hexahydropyrimidin-1-yl)ethyl] carbamate
State
State

At room temperature, the compound is typically in a solid state.

Melting point (Celsius)
192.00
Melting point (Kelvin)
465.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
400.46g/mol
Molar mass
400.4560g/mol
Density
1.3200g/cm3
Appearence

The compound typically appears as a fluffy white powder or solid.

Comment on solubility

Solubility of 1-(butoxymethyl)-2-(5-ethyl-2,4,6-trioxo-5-phenyl-hexahydropyrimidin-1-yl)ethyl carbamate

The solubility of the compound 1-(butoxymethyl)-2-(5-ethyl-2,4,6-trioxo-5-phenyl-hexahydropyrimidin-1-yl)ethyl carbamate can be quite complex due to its structure. Here are some key factors that influence its solubility:

  • Polarity: This compound features both polar and non-polar functional groups, which can affect its solubility in various solvents.
  • Hydrophilicity vs. Hydrophobicity: It possesses hydrophilic carbamate groups that may enhance solubility in aqueous solutions, while the butoxy groups may increase hydrophobic characteristics.
  • Temperature: The solubility may vary significantly with temperature changes, potentially allowing for increased solubility at elevated temperatures.
  • Solvent Choice: Solubility is highly dependent on the solvent; it may show greater solubility in polar organic solvents compared to nonpolar solvents.

It is important to note that due to these factors, the solubility of the compound can be categorized as:

  1. Moderate in polar solvents
  2. Low in nonpolar solvents

In summary, understanding the solubility characteristics of this compound is crucial for its application in chemical formulations, ensuring the right solvent blend is chosen for optimal performance.

Interesting facts

Interesting Facts About 1-(Butoxymethyl)-2-(5-Ethyl-2,4,6-Trioxo-5-Phenyl-Hexahydropyrimidin-1-Yl)Ethyl Carbamate

This compound belongs to a fascinating class of compounds known as carbamates, which are esters or salts of carbamic acid. Carbamates have gained attention in various fields due to their versatile applications, particularly in pharmaceuticals and agrochemicals.

Key Highlights:

  • Pharmaceutical Potential: The unique structure of this compound suggests possible bioactivity, making it a candidate for development as a pharmaceutical agent. Structures similar to this have been explored for their ability to exhibit therapeutic effects, ranging from anti-inflammatory to anticancer properties.
  • Synthesis Challenges: The synthetic pathway to create this compound is likely complex, as it incorporates multiple functional groups and cyclic structures. Such intricate syntheses often lead to interesting purification and characterization challenges for chemists.
  • Intermolecular Interactions: Due to the presence of multiple functional sites, this molecule can engage in various intermolecular interactions, such as hydrogen bonding, which can influence its biological activity and solubility.
  • Structure-Activity Relationship: Researchers are often interested in understanding how structural modifications can impact the activity of such compounds. This illustrates the critical concept of structure-activity relationship (SAR), which is central to drug design.

Quote from a Chemist: "The complexity of modern organic compounds opens new frontiers in medicinal chemistry, where every atom counts towards the overall efficacy of a drug."

In summary, 1-(butoxymethyl)-2-(5-ethyl-2,4,6-trioxo-5-phenyl-hexahydropyrimidin-1-yl)ethyl carbamate stands out not just for its intricate structure, but also for its potential implications in research and industry, making it a compound worth exploring further.

Synonyms
Febarbamate
phenobamate
Phebarbamate
Tymium
G-Tril
Febarbamato
Getril
Febarbamatum
Febarbamate [INN:DCF]
Febarbamatum [INN-Latin]
Febarbamato [INN-Spanish]
GO-560
EINECS 236-226-3
UNII-5Z48ONN38P
GO 560
Febarbamate (INN)
BRN 0591584
5Z48ONN38P
FEBARBAMATE [MI]
FEBARBAMATE [INN]
FEBARBAMATE [MART.]
FEBARBAMATE [WHO-DD]
DTXSID40864380
3-(3-Butoxy-3-carbamoyloxypropyl)-5-ethyl-5-phenylbarbituric acid
3-(gamma-Butoxy-beta-carbamyl-beta-propanol)-5-phenyl-5-ethylmalonylurea
5-24-09-00304 (Beilstein Handbook Reference)
1-(3-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenylbarbituric acid carbamate ester
1-(3-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenylbarbituric acid, carbamate ester
1-(3-butoxy-2-carbamoyloxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trione
Barbituric acid, 1-(3-butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-, carbamate (ester)
Carbamic acid, ester with 1-(3-butoxy-2-hydroxypropyl)-5-ethyl-5-phenylbarbituric acid
Febarbamatum (INN-Latin)
Febarbamato (INN-Spanish)
FEBARBAMATE (MART.)
1-Butoxy-3-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)propan-2-yl carbamate
5-ethyl-1-(3-butoxy-2-carbamoyloxypropyl)-5-barbituric acid
DTXCID20812905
M03BA05
236-226-3
13246-02-1
[1-butoxy-3-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)propan-2-yl] carbamate
SCHEMBL18473
CHEMBL2104283
SCHEMBL27835181
CHEBI:135655
QHZQILHUJDRDAI-UHFFFAOYSA-N
DB13303
NS00005989
D07275
Q5439707