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Ethyl isopropylcarbamate

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Identification
Molecular formula
C7H15NO2
CAS number
13257-54-0
IUPAC name
ethyl N-isopropylcarbamate
State
State

At room temperature, ethyl isopropylcarbamate is a liquid.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
176.00
Boiling point (Kelvin)
449.15
General information
Molecular weight
145.21g/mol
Molar mass
145.1830g/mol
Density
0.9705g/cm3
Appearence

Ethyl isopropylcarbamate typically appears as a colorless to pale yellow liquid. Its appearance may vary slightly depending on the purity and presence of impurities.

Comment on solubility

Solubility of Ethyl N-isopropylcarbamate

Ethyl N-isopropylcarbamate, with the chemical formula C5H11N1O2, presents an intriguing profile when it comes to solubility. This compound is primarily soluble in organic solvents but tends to have limited solubility in water. Here are some key points regarding its solubility:

  • Organic Solvents: Ethyl N-isopropylcarbamate readily dissolves in solvents such as ethanol, acetone, and chloroform.
  • Water Solubility: The polar nature of the carbamate group contributes to its limited solubility in water, typically requiring elevated temperatures or specific conditions to improve solubility.
  • Influencing Factors: Factors such as pH, temperature, and the presence of cosolvents can significantly influence the compound's solubility in aqueous solutions.

Overall, understanding the solubility characteristics of ethyl N-isopropylcarbamate is essential for its applications in various chemical processes and formulations. As stated, "Solubility is key to reactivity," highlighting how the solubility of this compound can directly impact its usability in practical applications.

Interesting facts

Interesting Facts about Ethyl N-Isopropylcarbamate

Ethyl N-isopropylcarbamate is a fascinating compound with a variety of applications in organic chemistry and medicinal fields. Here are some intriguing points about this compound:

  • Structure and Function: Ethyl N-isopropylcarbamate contains an isopropyl group attached to a carbamate moiety. This unique structure lends the compound its distinct properties and contributes to its function as an important building block in synthesizing other complex molecules.
  • Biological Activity: This compound exhibits interesting biological activity, making it a subject of interest in pharmacological research. Studies have suggested that it may have potential applications in drug delivery systems and agricultural chemicals.
  • Synthesis: The synthesis of ethyl N-isopropylcarbamate can be achieved through various methods, typically involving the reaction of isopropylamine with an ethyl carbamate. This pathway exemplifies the importance of amine and carbamate chemistry in organic synthesis.
  • Analytical Techniques: Due to its diverse applications, it is critical to utilize advanced analytical techniques such as NMR spectroscopy and mass spectrometry for studying this compound. These methods allow chemists to determine purity and validate the compound’s structure.
  • Environmental Significance: Understanding the environmental impacts of derivatives of carbamate compounds, including ethyl N-isopropylcarbamate, is essential. Continuous research is being conducted to evaluate its behavior and persistence in the environment, particularly as it relates to agricultural use.

In the world of chemistry, compounds like ethyl N-isopropylcarbamate represent the interconnectedness of structure and function. As research continues to unfold, who knows what new applications and properties we may discover!

Synonyms
Ethyl isopropylcarbamate
2594-20-9
Isopropyl ethyl urethan
ethyl N-propan-2-ylcarbamate
CARBAMIC ACID, ISOPROPYL-, ETHYL ESTER
ethyl (1-methylethyl)carbamate
Carbamic acid, (1-methylethyl)-, ethyl ester
LP6CSR4YU7
isopropyl-carbamic acid ethyl ester
NSC-29184
Carbamic acid, N-(1-methylethyl)-, ethyl ester
NSC 29184
BRN 1750035
AI3-16944
Isopropyl urethane
UNII-LP6CSR4YU7
SCHEMBL906813
WLN: 2OVMY1&1
ETHYL N-ISOPROPYLCARBAMATE
DTXSID90180603
JGRPZAGOYKNIAC-UHFFFAOYSA-N
N-ISOPROPYL-O-ETHYLURETHANE
NSC29184
AKOS003849799
DS-007405
Carbamic acid,(1-methylethyl)-, ethyl ester (9ci)