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(2-chloroacetyl) 2-chloroacetate

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Identification
Molecular formula
C4H5Cl2O3
CAS number
621-86-9
IUPAC name
(2-chloroacetyl) 2-chloroacetate
State
State

At room temperature, (2-chloroacetyl) 2-chloroacetate is a liquid.

Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
172.30
Boiling point (Kelvin)
445.45
General information
Molecular weight
157.46g/mol
Molar mass
157.4550g/mol
Density
1.4510g/cm3
Appearence

(2-chloroacetyl) 2-chloroacetate appears as a colorless to pale yellow liquid. It can exhibit a strong and pungent odor, resulting from its reactive acyl chloride functional group.

Comment on solubility

Solubility of (2-chloroacetyl) 2-chloroacetate

(2-chloroacetyl) 2-chloroacetate, a compound known for its interesting chemical properties, demonstrates specific solubility characteristics that are vital for its applications. Understanding solubility can inform scientists about how this compound interacts in various environments. Here are some important points to consider regarding its solubility:

  • Polar Characteristics: Due to the presence of polar functional groups in the molecule, (2-chloroacetyl) 2-chloroacetate is likely to be soluble in polar solvents, such as water and alcohols.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature—often resulting in better dissolution in warmer solvents.
  • Interaction with Non-Polar Solvents: It is less soluble in non-polar solvents due to the hydrophilic nature of the chlorinated acetyl groups, limiting its usefulness in those environments.

In conclusion, the solubility behavior of (2-chloroacetyl) 2-chloroacetate makes it a fascinating subject of study. It serves as a reminder of the complex interplay between molecular structure and solvent interactions, emphasizing that solubility is not simply a matter of "like dissolving like" but also influenced by various chemical features and conditions.

Interesting facts

Interesting Facts About (2-chloroacetyl) 2-chloroacetate

(2-chloroacetyl) 2-chloroacetate is a fascinating compound that showcases the intersection of organic chemistry and practical application. Known for its **role in organic synthesis**, this compound can be utilized in various chemical reactions, providing pathways to synthesize more complex molecules. Here are some intriguing insights into this compound:

  • Preparation: It can be synthesized through a reaction involving acetyl chloride and chloroacetic acid, demonstrating a typical process in organic chemistry.
  • Reactivity: Due to the presence of electronegative chlorine atoms, this compound exhibits significant electrophilic properties, making it valuable in the formation of esters and other derivatives.
  • Industrial Use: It finds applications in the development of pharmaceuticals and agrochemicals, highlighting its importance in the chemical industry.
  • Mechanisms: Studying its reactions can provide insights into **nucleophilic substitution mechanisms**, a foundational concept in organic chemistry.
  • Derivatives: Research into derivatives of (2-chloroacetyl) 2-chloroacetate can lead to new chemical entities with potential *biological activity*.

A notable characteristic of this compound is the versatility that halogenated compounds like it offer in synthetic methodologies. As a chemist, understanding such compounds enhances one’s ability to manipulate molecular structures, ultimately contributing to advancements in fields such as drug design and material science.

Overall, (2-chloroacetyl) 2-chloroacetate exemplifies a compound where fundamental chemistry merges with practical outcomes, making it a subject of interest for both chemistry students and experienced scientists alike.

Synonyms
Chloroacetic anhydride
541-88-8
Monochloroacetic acid anhydride
CHLORACETIC ANHYDRIDE
2-Chloroacetic anhydride
Chloroacetyl anhydride
Chloroacetic acid anhydride
Chloroethanoic anhydride
Acetic acid, chloro-, anhydride
Sym-dichloroacetic anhydride
8Q7TXH7R5F
HSDB 5685
EINECS 208-794-2
alpha,alpha'-Dichloroacetic anhydride
NSC 71207
NSC-71207
Acetic acid, 2-chloro-, 1,1'-anhydride
AI3-52321
EC 208-794-2
DTXSID701014649
CHLOROACETIC ANHYDRIDE [MI]
CHLOROACETIC ANHYDRIDE [HSDB]
2Chloroacetic anhydride
Symdichloroacetic anhydride
Acetic acid, chloro, anhydride
DTXCID80818307
alpha,alpha'Dichloroacetic anhydride
208-794-2
(2-chloroacetyl) 2-chloroacetate
Monochloroacetic anhydride
MFCD00000929
UNII-8Q7TXH7R5F
Bischloroacetic Acid) Anhydride; Chloroacetic Acid Anhydride; Chloroacetic Anhydride; alpha,alpha'-Dichloroacetic Anhydride; NSC 71207
chioroacetic anhydride
chloro acetic anhydride
(ClCH2CO)2O
Chloroacetic anhydride, tech
NCIOpen2_000530
SCHEMBL16026
Chloroacetic anhydride, 95%
PNVPNXKRAUBJGW-UHFFFAOYSA-
NSC71207
STL185629
AKOS005207079
LS-12974
NS00003284
Q27270893
F0001-1424
InChI=1/C4H4Cl2O3/c5-1-3(7)9-4(8)2-6/h1-2H2