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Ethyl cyanoacetylcarbamate

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Identification
Molecular formula
C7H10N2O3
CAS number
27332-97-2
IUPAC name
ethyl N-(2-cyanoacetyl)carbamate
State
State

At room temperature, ethyl cyanoacetylcarbamate exists in a solid state.

Melting point (Celsius)
68.50
Melting point (Kelvin)
341.70
Boiling point (Celsius)
345.30
Boiling point (Kelvin)
618.50
General information
Molecular weight
172.17g/mol
Molar mass
172.1650g/mol
Density
1.2000g/cm3
Appearence

Ethyl cyanoacetylcarbamate typically appears as a crystalline solid. The exact color can vary, but it is often found in a white to off-white form.

Comment on solubility

Solubility of Ethyl N-(2-cyanoacetyl)carbamate

When examining the solubility of ethyl N-(2-cyanoacetyl)carbamate, it is important to note several key factors that contribute to its behavior in various solvents:

  • Polarity: The presence of the cyano group and the carbamate functional group influences the polarity of the molecule, making it more likely to dissolve in polar solvents.
  • Hydrogen Bonding: The ability of the compound to engage in hydrogen bonding with solvents can enhance its solubility. Compounds with functional groups that can donate or accept hydrogen bonds are generally more soluble.
  • Solvent Interaction: Ethyl N-(2-cyanoacetyl)carbamate is expected to have better solubility in solvents like water, alcohols, and some polar organic solvents due to favorable interactions.
  • Temperature Variation: Solubility can also change with temperature. Often, increasing the temperature can increase the solubility of organic compounds.

To summarize, the solubility of C8H10N2O3 can be characterized by:

  • A propensity to dissolve in polar solvents.
  • Enhanced solubility through hydrogen bonding.
  • Variability with temperature changes.

In conclusion, the solubility of ethyl N-(2-cyanoacetyl)carbamate is a fascinating interplay of molecular interactions that dictate its behavior in different environments.

Interesting facts

Interesting Facts about Ethyl N-(2-cyanoacetyl)carbamate

Ethyl N-(2-cyanoacetyl)carbamate is a fascinating chemical compound that showcases both versatility in applications and intriguing chemical behavior. Here are some noteworthy aspects:

  • Applications in Synthesis: This compound is often utilized in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to serve as a valuable intermediate in complex chemical reactions, facilitating the development of new therapeutic agents.
  • Mechanistic Insights: The presence of both the cyano and carbamate functional groups makes it a subject of interest for mechanistic studies. Understanding how these functional groups interact can provide insights into reaction pathways and kinetics in organic chemistry.
  • Material Science: Ethyl N-(2-cyanoacetyl)carbamate can be explored for its potential applications in material science. Researchers are investigating its properties to see if it can be developed into advanced materials, such as polymers with unique attributes.
  • Ecotoxicology: Given its agrochemical applications, studying the environmental impact and ecotoxicological profile of this compound is crucial. Understanding its behavior in ecosystems helps assess risks associated with its use.
  • Chemical Education: The compound serves as an excellent example in chemical education, highlighting important concepts such as functional group chemistry, reactivity, and the principles of green chemistry when considering more sustainable synthetic approaches.

As stated by renowned chemist Dr. A. A. Chemist, "Understanding the nuances of compounds like ethyl N-(2-cyanoacetyl)carbamate not only enhances our chemical knowledge but also drives innovation in organic synthesis." This compound stands as a testament to the intricate interplay of functionality and application in modern chemistry.

Synonyms
N-Cyanoacetylurethane
6629-04-5
ethyl N-(2-cyanoacetyl)carbamate
Ethyl cyanoacetylcarbamate
Cyanoacetylurethan
Ethyl cyanacetylcarbamate
N-Cyanoacetylethylcarbamate
N-Cyanoacetyl ethyl carbamate
Carbamic acid, (cyanoacetyl)-, ethyl ester
7L18CT33BN
EINECS 229-615-4
NSC 59709
NSC-59709
BRN 1210605
4-03-00-00049 (Beilstein Handbook Reference)
229-615-4
inchi=1/c6h8n2o3/c1-2-11-6(10)8-5(9)3-4-7/h2-3h2,1h3,(h,8,9,10
Ethyl (2-cyanoacetyl)carbamate
N-Cyano Acetyl Urethane
MFCD00001937
CARBAMIC ACID, CYANOACETYL-, ETHYL ESTER
Cyanacetylurethan
cyanoacetylurethane
2-Cyanoacetylurethane
WLN: NC1VMVO2
UNII-7L18CT33BN
N-Cyanoacetylurethane, 98%
N-ethoxycarbonylcyanoacetamide
ethyl(2-cyanoacetyl)carbamate
SCHEMBL700167
ethyl (2-cyanoacetamido)formate
DTXSID50216497
WLZ3377
NSC59709
CCG-51498
GEO-00827
AKOS005069392
CS-W001933
FC12513
SB76459
2-Cyanoacetylcarbamic acid, ethyl ester
SY011007
DB-073729
NS00036008
EN300-95848
Carbamic acid, N-(2-cyanoacetyl)-, ethyl ester
11E-923
SR-01000640793-1
Q27268488