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2-Chloropropionic acid

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Identification
Molecular formula
C3H5ClO2
CAS number
598-78-7
IUPAC name
2-chloropropanoic acid
State
State

2-Chloropropionic acid is typically in a liquid state at room temperature due to its relatively low melting point of 11.5 °C.

Melting point (Celsius)
11.50
Melting point (Kelvin)
284.65
Boiling point (Celsius)
187.00
Boiling point (Kelvin)
460.15
General information
Molecular weight
108.52g/mol
Molar mass
108.5200g/mol
Density
1.2480g/cm3
Appearence

2-Chloropropionic acid is a colorless liquid. It is hygroscopic, meaning it absorbs moisture from the air. It has a pungent odor and is corrosive.

Comment on solubility

Solubility of 2-Chloropropanoic Acid

2-Chloropropanoic acid, with the chemical formula C3H7ClO2, exhibits interesting solubility characteristics that are important in various chemical applications.

Here are some key points regarding its solubility:

  • Polar Nature: The presence of the carboxylic acid group (-COOH) contributes to the compound's polar nature, enhancing its ability to interact with water molecules.
  • Solubility in Water: 2-Chloropropanoic acid is soluble in water, which means it can readily dissolve and form solutions, particularly at higher temperatures.
  • Organic Solvents: It is also soluble in many organic solvents, including ethanol and ether, making it versatile in different solvent systems.
  • Temperature Effects: Like many organic acids, its solubility can increase with temperature, which can be beneficial for reactions that require the compound in solution.

To summarize, "2-Chloropropanoic acid is a soluble compound in both aqueous and organic environments," emphasizing its usefulness in various chemical processes and reactions. Understanding its solubility helps in predicting its behavior in different systems and applications.

Interesting facts

Interesting Facts About 2-Chloropropanoic Acid

2-Chloropropanoic acid, a derivative of propanoic acid, is not only notable for its unique structure but also for its various applications in the field of organic chemistry. Here are some intriguing aspects of this compound:

  • Structure and Isomerism: The presence of the chlorine atom at the second carbon of the propanoic acid skeleton introduces a significant amount of stereochemistry. Unlike its isomer, 1-chloropropanoic acid, 2-chloropropanoic acid exhibits distinctive reactivity and properties due to the positioning of the halogen.
  • Reactivity: The acidic nature of 2-chloropropanoic acid makes it an excellent candidate for various chemical reactions, including esterification and decarboxylation. It can be involved in nucleophilic substitution reactions due to the presence of a leaving group (chlorine).
  • Biological Relevance: This compound has shown potential as a building block in the synthesis of pharmaceutical agents. Its derivatives may exhibit unique biological activities, contributing to drug discovery and development.
  • Industrial Applications: 2-Chloropropanoic acid is utilized in the production of agrochemicals, dyes, and other specialty chemicals. Its ability to modify organic molecules opens up avenues for diverse industrial applications.
  • Synthesis: Chemists can synthesize this compound through various methods, one of which involves the chlorination of propanoic acid. This process highlights the importance of halogenated compounds in organic synthesis.

As a fascinating example of how a single substitution can dramatically alter the properties and applications of a compound, 2-chloropropanoic acid serves as a case study in the realm of organic chemistry. It emphasizes the importance of understanding molecular structure in predicting reactivity and promising applications.

Synonyms
2-Chloropropionic acid
2-CHLOROPROPANOIC ACID
598-78-7
Propanoic acid, 2-chloro-
UNII-ADV1WUE1NB
HSDB 5713
NSC 173
EINECS 209-952-3
UN2511
BRN 1720259
DTXSID0021545
AI3-18182
NSC-173
2-chloroproprionic acid
DTXCID301545
EC 209-952-3
0-02-00-00248 (Beilstein Handbook Reference)
(RS)-2-CHLOROPROPANOIC ACID
(RS)-2-CHLOROPROPIONIC ACID
2-CHLOROPROPANOIC ACID [WHO-DD]
(+-)-2-Chloropropanoic acid
2chloropropanoic acid
alphaChloropropionic acid
Propanoic acid, 2chloro
Propionic acid, 2chloro
Propionic acid, alphachloro
alphaMonochloropropionic acid
DL-2-CHLOROPROPIONIC ACID
(+-)-2-CHLOROPROPIONIC ACID
(RS)-ALPHA-CHLOROPROPIONIC ACID
(+-)-ALPHA-CHLOROPROPANOIC ACID
(.+-.)-2-CHLOROPROPANOIC ACID
(.+-.)-2-CHLOROPROPIONIC ACID
(.+-.)-ALPHA-CHLOROPROPANOIC ACID
209-952-3
(+-)-.alpha.-chloropropanoic acid
.alpha.-chloropropionic acid, (+-)-
alpha-chloropropionic acid, (+-)-
gawayyrqgqzkcr-uhfffaoysa-n
Propionic acid, 2-chloro-
(S)-(-)-2-Chloropropionic acid
alpha-Chloropropionic acid
R(+)-2-Chloropropionic acid
.alpha.-Chloropropionic acid
(+/-)-2-Chloropropionic acid
Propionic acid, .alpha.-chloro-
2-Chloropropionate
ADV1WUE1NB
(+/-)-2-CHLOROPROPANOIC ACID
Propanoic acid, chloro-
.alpha.-Monochloropropionic acid
Chloropropionic acid
28554-00-9
(+/-)-.ALPHA.-CHLOROPROPANOIC ACID
.ALPHA.-CHLOROPROPIONIC ACID, (+/-)-
alpha-Monochloropropionic acid
Propionic acid, alpha-chloro-
(R)-(+)-2-ChloropropionicAcid
MFCD00064205
CH3CHClCOOH
2-chloro-propionic acid
WLN: QVYG1
alpha-chloro-propionic acid
NCIOpen2_009382
SCHEMBL24339
S(-)-2-Chloropropionic acid
2-Chloropropionic acid, 92%
NSC173
CHEMBL1743205
(S)-(-)-2-ChloropropionicAcid
(RS)-(+)-2-chloropropionic acid
BCP11281
STR00768
Tox21_200650
(+)-2-Chloropropionic acid, 94%
MFCD00004224
NSC401806
AKOS000121295
AKOS016843695
NSC-401806
NCGC00258204-01
(+/-)-ALPHA-CHLOROPROPANOIC ACID
62138-52-7
CAS-598-78-7
SY018972
DB-353182
ALPHA-CHLOROPROPIONIC ACID, (+/-)-
NS00006498
EN300-22778
2-Chloropropionic acid [UN2511] [Corrosive]
Q209361
(R)-2-chloropropanoic acid;D-2-Chloropropionic acid
F2190-0290
Z147646840