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Ethyl isocarbamate

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Identification
Molecular formula
C4H7NO2
CAS number
109-90-0
IUPAC name
ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate
State
State

In its natural state at room temperature, ethyl isocyanate is a liquid. Proper storage conditions must be maintained to prevent it from reacting with atmospheric moisture or decomposing.

Melting point (Celsius)
-99.00
Melting point (Kelvin)
174.15
Boiling point (Celsius)
92.00
Boiling point (Kelvin)
365.15
General information
Molecular weight
99.10g/mol
Molar mass
99.0960g/mol
Density
1.0140g/cm3
Appearence

Ethyl isocyanate is a colorless to yellow liquid. It is typically clear and has a pungent odor characteristic of isocyanates. Due to its reactive nature, it should be handled in a controlled environment to avoid any reactions with moisture or other chemicals.

Comment on solubility

Solubility Characteristics of Ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate

When it comes to the solubility of ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate, several factors play a significant role. This compound possesses unique structural features that can influence its solubility behavior in various solvents. Below are some key points to consider:

  • Polarity: The presence of a carbamate functional group can impart some degree of polarity to the molecule, potentially allowing for solubility in polar solvents like water or alcohols.
  • Hydrophobic Characteristics: The tricyclo[2.2.1.02,6]heptanyl moiety is largely hydrophobic, which may limit the overall solubility of the compound in aqueous solutions.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetone compared to polar solvents.
  • Temperature Effects: The solubility may increase with temperature, as is common with many organic compounds, thus enhancing dissolution in organic solvents at elevated temperatures.

In summary, the solubility of ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate can be characterized by a balance of its polar and non-polar characteristics, affecting its interaction with different solvents. Understanding these solubility profiles is essential for applications in various fields, such as pharmaceuticals or organic synthesis.

Interesting facts

Interesting Facts about Ethyl N-(3-Tricyclo[2.2.1.02,6]heptanyl)carbamate

Ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate is a fascinating compound within the realm of organic chemistry, primarily due to its unique structural features and potential applications in various fields. Here are some intriguing facts about this compound:

  • Unique Structure: This compound contains a tricyclic structure, which consists of three interconnected rings. Such structures often exhibit interesting properties and can be categorized as fused bicyclic or tricyclic compounds, adding to the complexity of their chemistry.
  • Potential Uses: Compounds with carbamate functional groups, like this one, are known for their diverse applications. They can act as insecticides, herbicides, or fungicides, thus holding significant importance in agricultural chemistry.
  • Synthetic Pathways: The synthesis of compounds containing tricyclic structures often involves intricate reactions, which can require multiple steps. This complexity can also offer chemists opportunities to explore new synthetic methods and optimize existing ones.
  • Biological Activity: Research indicates that certain tricyclic compounds can exhibit biological activity, potentially leading to the development of novel pharmaceuticals. The unique stereo and electronic properties of this compound can influence its interactions with biological targets.
  • Historical Context: Tricyclic compounds have a rich history in medicinal chemistry, particularly noted for their role in the development of antidepressants. Understanding how related structures function could open avenues for creating new therapeutic agents.
  • Material Science: Beyond biological applications, compounds like ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate may find utility in material science due to their potential for forming polymers or other relevant materials with specific functionalities.

In summary, the study of ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate not only expands our understanding of organic chemistry but also paves the way for potential innovations in various scientific fields. As the exploration of such complex compounds continues, the possible real-world applications make this an exciting area of study!

Synonyms
Ethyl 3-nortricyclylcarbamate
709-70-6
3-Nortricyclenecarbamic acid, ethyl ester
NSC 102512
BRN 2805088
Tricyclo(2.2.1.02,6)heptane-3-carbamic acid, ethyl ester
Carbamic acid, tricyclo(2.2.1.02,6)hept-3-yl-, ethyl ester
CARBAMIC ACID, N-(TRICYCLO(2.2.1.0(sup 2,6))HEPTAN-3-YL)-, ETHYL ESTER
Tricyclo[2.2.1.0(2,6)]heptane-3-carbamic acid, ethyl ester
Carbamic acid, tricyclo[2.2.1.0(2,6)]hept-3-yl-, ethyl ester
Carbamic acid, N-(tricyclo(2.2.1.0(sup2,6))heptan-3-yl)-, ethyl ester
Tricyclo(2.2.1.0(2,6))heptane-3-carbamic acid, ethyl ester
Carbamic acid, tricyclo(2.2.1.0(2,6))hept-3-yl-, ethyl ester
Tricyclo(2.2.1.02,6)heptane-3-carbamic acid, ethyl ester (8CI)
Carbamic acid, tricyclo(2.2.1.02,6)hept-3-yl-, ethyl ester (9CI)
nsmnojjqbxbpgs-uhfffaoysa-n
ethyl N-(3-tricyclo[2.2.1.02,6]heptanyl)carbamate
ethyl N-{tricyclo[2.2.1.0?,?]heptan-3-yl}carbamate
N-(Tricyclo[2.2.1.02,6]heptan-3-yl)carbamic acid ethyl ester
DTXSID20991188
Tricyclo[2.2.1.02, ethyl ester
NSC102512
AKOS024332992
NSC-102512
Carbamic acid,6]hept-3-yl-, ethyl ester
Carbamic acid,6)]heptan-3-yl)-, ethyl ester
ethyl tricyclo[2.2.1.0~2,6~]hept-3-ylcarbamate
Ethyl hydrogen tricyclo[2.2.1.0~2,6~]heptan-3-ylcarbonimidate