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Methyl N-carbamoylcarbamate

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Identification
Molecular formula
C3H6N2O3
CAS number
315-18-4
IUPAC name
methyl N-carbamoylcarbamate
State
State

At room temperature, Methyl N-carbamoylcarbamate is typically found in a solid crystalline state.

Melting point (Celsius)
97.00
Melting point (Kelvin)
370.15
Boiling point (Celsius)
198.00
Boiling point (Kelvin)
471.15
General information
Molecular weight
133.09g/mol
Molar mass
133.0920g/mol
Density
1.3910g/cm3
Appearence

Methyl N-carbamoylcarbamate typically appears as a solid crystalline substance. It is white in color and can exist in powder or crystalline form.

Comment on solubility

Solubility of Methyl N-carbamoylcarbamate

Methyl N-carbamoylcarbamate, with the chemical formula C4H8N2O3, exhibits notable solubility characteristics that are influenced by its molecular structure. Understanding the solubility of this compound can be crucial for its applications in various fields, including pharmaceuticals and agriculture. Here are some key points regarding its solubility:

  • Solvent Compatibility: Methyl N-carbamoylcarbamate is generally soluble in polar solvents like water and alcohols due to its ability to form hydrogen bonds.
  • Temperature Dependence: The solubility of this compound can increase with temperature, which is a common trait among many organic compounds.
  • pH Sensitivity: The solubility can also be pH dependent, with higher solubility often observed in acidic conditions compared to neutral or basic environments.

In summary, Methyl N-carbamoylcarbamate's solubility is relatively favorable in polar solvents, which enhances its potential for use in various chemical processes. As the saying goes, "Like dissolves like," meaning that similar polar compounds tend to be soluble in one another, thus impacting the practical applications of methyl N-carbamoylcarbamate in solution-based systems.

Interesting facts

Interesting Facts about Methyl N-carbamoylcarbamate

Methyl N-carbamoylcarbamate, sometimes referred to as a derivative of carbamic acid, is a fascinating compound with unique properties and applications, particularly in the field of organic chemistry. This compound is known for its role as an intermediate in the synthesis of various pesticides and pharmaceutical compounds. Here are several intriguing aspects of methyl N-carbamoylcarbamate:

  • Biological Relevance: Compounds like methyl N-carbamoylcarbamate have been studied for their potential biological activity, revealing interesting interactions with enzymes and possible uses in medicinal chemistry.
  • Versatile Synthesis: This compound can be synthesized through diverse organic reactions, showcasing the versatility of carbamates in synthetic chemistry.
  • Research Applications: It serves as a valuable building block in organic synthesis, particularly in the development of agrochemicals, which are crucial for modern agriculture.
  • Environmental Considerations: As with many chemicals, understanding the behavior and fate of methyl N-carbamoylcarbamate in the environment is crucial, particularly given the agricultural applications that can impact ecosystems.
  • Historical Perspectives: The study of carbamates dates back several decades, contributing to the understanding of chemical reactivity and functional groups in organic compounds.

Overall, methyl N-carbamoylcarbamate exemplifies the blend of theoretical and practical aspects of chemistry, highlighting its importance in both academic research and industrial applications. As scientists continue to explore and develop new derivatives, the potential uses of this compound are likely to expand even further.

Synonyms
methyl N-carbamoylcarbamate
Methyl allophanate
Methyl N-(aminocarbonyl)carbamate
9HK6V636PF
NSC-48290
CARBAMIC ACID, N-(AMINOCARBONYL)-, METHYL ESTER
684-746-8
761-89-7
Carbomethoxyurea
allophanic acid methyl ester
ALLOPHANIC ACID, METHYL ESTER
USAF EL-70
methylcarbamoylcarbamate
1-(Methoxycarbonyl)urea
methyl carbamoylcarbamate
Carbamic acid,(aminocarbonyl)-, methyl ester (9CI)
Methyl (aminocarbonyl)carbamate
NSC 48290
BRN 1758683
Carbamic acid, carbamoyl-, methyl ester
Carbamic acid, (aminocarbonyl)-, methyl ester
allophanate methyl ester
WLN: ZVMVO1
UNII-9HK6V636PF
4-03-00-00127 (Beilstein Handbook Reference)
SCHEMBL376341
CHEBI:2600
DTXSID20226982
NSC48290
STL280256
AKOS005208672
N-Aminocarboxyl-carbamic acid methyl ester
Q27105730