Interesting facts
              Interesting Facts about 3-Chloropropanoic Acid
3-Chloropropanoic acid is a fascinating compound that belongs to the family of carboxylic acids, which are known for their wide range of applications in various fields. Here are some intriguing aspects of this compound:
- Source of Derivatives: This compound serves as a valuable starting material for synthesizing numerous derivatives, including various pharmaceutical agents and agrochemicals. Its unique structure allows for modifications that enhance biological activity.
 - Biological Activity: 3-Chloropropanoic acid has been studied for its potential antimicrobial and herbicidal properties. Research indicates that compounds with chlorine substitutions often exhibit heightened biological effects.
 - Industrial Uses: In addition to its role in organic synthesis, this compound is utilized in the production of various chemicals that find application in manufacturing and research.
 - Environmental Impact: As with many halogenated compounds, 3-chloropropanoic acid raises concerns about environmental persistence and toxicity. Understanding its behavior in nature is critical for assessing its ecological impact.
 - Safety Precautions: Being a corrosive substance, 3-chloropropanoic acid requires careful handling. Laboratory workers must always wear appropriate personal protective equipment (PPE) to prevent skin and eye contact.
 
Overall, 3-chloropropanoic acid exemplifies how seemingly simple compounds can have complex chemical behavior and significant implications in both scientific research and practical applications. As a student or scientist, exploring the properties and reactions of this compound can open up numerous avenues for inquiry and innovation.
Synonyms
          3-CHLOROPROPIONIC ACID
          3-Chloropropanoic acid
          107-94-8
          Propanoic acid, 3-chloro-
          Propionic acid, 3-chloro-
          beta-Chloropropionic acid
          3-Chloropropanic acid
          .beta.-Chloropropionic acid
          beta-Monochloropropionic acid
          3-chloro-propionic acid
          HSDB 2053
          NSC 174
          EINECS 203-534-4
          BRN 1098495
          CCRIS 9440
          R5J180FN9Z
          DTXSID5021546
          AI3-22338
          NSC-174
          DTXCID701546
          .beta.-Monochloropropionic acid
          EC 203-534-4
          3-CHLOROPROPIONIC ACID [HSDB]
          .BETA.-CHLOROPROPIONIC ACID [MI]
          WLN: QV2G
          UNII-R5J180FN9Z
          3-chloropropionate
          R-Chloropropionate
          3chloropropanoic acid
          3-monochloropropionate
          betaChloropropionic acid
          chloromethyl acetic acid
          Propanoic acid, 3chloro
          Propionic acid, 3chloro
          betaMonochloropropionic acid
          UMB66
          SCHEMBL139248
          3-Chloropropionic acid, 98%
          NSC174
          CHEMBL1990700
          NSC2183
          NSC-2183
          Tox21_201185
          BBL012215
          MFCD00002764
          STL163556
          AKOS005287338
          FC34154
          NCGC00248950-01
          NCGC00258737-01
          AC-16131
          CAS-107-94-8
          NCI60_001817
          VS-03236
          CS-0165952
          NS00007507
          EN300-24953
          Q223070
          3-chloropropanoic acid? (Brexpiprazole Impurity pound(c)
          F2191-0212
          Z203045320
          203-534-4
              
Solubility of 3-chloropropanoic acid
3-chloropropanoic acid, with the chemical formula C3H5ClO2, exhibits intriguing solubility properties, characteristic of many carboxylic acids. This compound is known to be soluble in water, making it useful in various aqueous applications. The solubility can be attributed to several factors:
As a general observation, carboxylic acids with fewer than five carbon atoms tend to be highly soluble in water. This behavior is ideal for laboratory applications where 3-chloropropanoic acid can be effectively utilized in synthesis and formulation processes.
In summary, the solubility of 3-chloropropanoic acid can be described as favorable due to its chemical structure and functional groups, enabling it to dissolve well in polar solvents like water.