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2-Chloroethyl acrylate

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Identification
Molecular formula
C5H7ClO2
CAS number
107-95-9
IUPAC name
2-chloroethyl prop-2-enoate
State
State

At room temperature, 2-chloroethyl acrylate is in a liquid state.

Melting point (Celsius)
-62.00
Melting point (Kelvin)
211.15
Boiling point (Celsius)
156.00
Boiling point (Kelvin)
429.15
General information
Molecular weight
136.58g/mol
Molar mass
136.5760g/mol
Density
1.1581g/cm3
Appearence

2-Chloroethyl acrylate is a colorless to pale yellow liquid with a pungent odor. It can appear transparent, making it difficult to distinguish from water or other clear liquids.

Comment on solubility

Solubility of 2-chloroethyl prop-2-enoate

2-chloroethyl prop-2-enoate, with the chemical formula C5H7ClO2, presents some interesting characteristics regarding its solubility. Generally, solubility can be influenced by various factors including molecular structure and polarity. For this compound, consider the following:

  • Polarity: The presence of the chlorine atom introduces polar characteristics, which can enhance its solubility in polar solvents.
  • Functional Groups: The ester (-COO-) and vinyl groups in its structure may also facilitate solubility in organic solvents.
  • Common Solvents: It is typically soluble in organic solvents such as acetone and ethanol due to compatible polar interactions.
  • Water Solubility: However, its overall solubility in water is expected to be limited because of the hydrophobic alkyl chain present.

As a general rule, “like dissolves like”, meaning that polar substances tend to dissolve well in polar solvents while non-polar substances are better soluble in non-polar solvents. Thus, for practical applications, it is essential to consider these attributes when determining the solubility of 2-chloroethyl prop-2-enoate in various mediums.

Interesting facts

Interesting Facts about 2-Chloroethyl Prop-2-enoate

2-Chloroethyl prop-2-enoate is an intriguing chemical compound that plays significant roles in various industrial applications. Here are some noteworthy points about this compound:

  • Versatile Reactivity: This compound is notable for its reactivity, particularly due to the presence of the vinyl group (prop-2-enoate) attached to the chloroethyl moiety. It can undergo various chemical reactions, making it valuable in synthesizing more complex molecules.
  • Industrial Importance: 2-Chloroethyl prop-2-enoate is primarily used in the production of polymers and resins. Its functional groups allow for crosslinking in polymerization processes, which enhances the durability and performance of the final products.
  • Biochemical Investigations: In the realm of medicinal chemistry, this compound has attracted attention for its potential applications in drug design. The chloro group can influence the biological activity of molecules, facilitating the development of pharmaceutical agents.
  • Environmental Considerations: As with many chlorinated compounds, researchers are investigating the environmental impact of 2-chloroethyl prop-2-enoate. Understanding its behavior in aquatic and terrestrial ecosystems is crucial for assessing risks associated with its use and disposal.

In the words of researchers studying similar compounds: "The nature of reactivity within these classes of compounds can lead to innovative solutions in both materials science and medicine." This highlights the dual role that compounds like 2-chloroethyl prop-2-enoate can play in advancing technology and health.

Overall, 2-chloroethyl prop-2-enoate is a compound that encapsulates the interconnected nature of chemistry and its broad applications in both industrial contexts and scientific research.

Synonyms
2-CHLOROETHYL ACRYLATE
Chloroethyl acrylate
Acrylic acid, 2-chloroethyl ester
2-Propenoic acid, 2-chloroethyl ester
Ethanol, 2-chloro-, acrylate
beta-Chloroethyl acrylate
.beta.-Chloroethyl acrylate
NSC 18592
NSC 65162
Acrylic acid .beta.-chloroethyl ester
CCRIS 4765
XA9Y3IT710
DTXSID8024783
2-Chloroacrylic acid ethyl ester
2-Chlorethylester kyseliny akrylove
Acrylic acid beta-chloroethyl ester
EINECS 218-619-1
NSC-18592
NSC-65162
BRN 1749712
UNII-XA9Y3IT710
AI3-03183
DTXCID404783
2-Chlorethylester kyseliny akrylove [Czech]
CHLOROETHYL ACRYLATE, 2-
2-Chloroethyl ester of acrylic acid
3-02-00-01225 (Beilstein Handbook Reference)
2-CHLOROETHANOL ACRYLATE
ACRYLIC ACID, BETA-CHLOROETHYL ESTER
2-Propenoic acid, 2-chloroethyl ester (9CI)
2-PROPENOIC ACID, BETA-CHLOROETHYL ESTER
218-619-1
whbaynmeixutjv-uhfffaoysa-n
2206-89-5
2-chloroethyl prop-2-enoate
MFCD00045292
WLN: 2OVYGU1
WLN: G2OV1U1
NCIOpen2_000601
SCHEMBL14856
CHEMBL450171
NSC18592
NSC65162
Tox21_202897
AKOS006345933
NCGC00260443-01
SY226312
CAS-2206-89-5
DB-045780
NS00027042
F20423
Q27293747
2-Chloroethyl acrylate, contains >100 ppm MEHQ as inhibitor, 97%