Interesting facts
Interesting Facts about 2,2-Dichloroacetic Acid
2,2-Dichloroacetic acid is a fascinating compound that has captured the interest of chemists and biochemists alike due to its versatile applications and intriguing properties. Here are some key points to understand this compound better:
- Structure and Reactivity: The presence of two chlorine atoms at the 2-position of the acetic acid moiety significantly enhances the reactivity of this compound. This reactivity enables it to participate in various chemical reactions, making it a useful building block in organic synthesis.
- Biological Impact: 2,2-Dichloroacetic acid has gained attention in biomedical research, particularly for its role in cellular metabolism. It is known to inhibit certain enzymes, such as pyruvate dehydrogenase kinase, which affects how cells process carbohydrates and fats.
- Environmental Considerations: While this compound has utility in organic chemistry, its environmental impact cannot be overlooked. Its potential as a pollutant has raised questions regarding its persistence and toxicity in aquatic environments.
- Applications: Beyond its role in chemical research, 2,2-dichloroacetic acid is used in the production of herbicides and fungicides, showcasing its importance in agriculture. Furthermore, it has implications in the synthesis of pharmaceuticals, providing a pathway to develop more effective drugs.
- Historical Context: The compound was first synthesized in the early 20th century, and since then, its applications have expanded significantly, illustrating the ever-growing relationship between chemistry and practical applications.
As a compound straddling the line between beneficial applications and potential hazards, 2,2-dichloroacetic acid serves as a reminder of the complexity of chemical compounds and their broader effects on health and the environment. In the words of a famous chemist, "The chemistry of substances is the poetry of nature." This compound certainly embodies that poetry, revealing layers of interaction and significance in both laboratory and real-world contexts.
Synonyms
DICHLOROACETIC ACID
79-43-6
2,2-Dichloroacetic acid
Dichloracetic acid
Acetic acid, dichloro-
Dichloroethanoic acid
Urner's liquid
Dichlorethanoic acid
Bichloracetic acid
Bichloroacetic Acid
DCA (acid)
DICHLORO-ACETIC ACID
Acetic acid, 2,2-dichloro-
Kyselina dichloroctova
NSC 2654
Dichloroacetic acid (IUPAC)
Kyselina dichloroctova [Czech]
CCRIS 4016
HSDB 6894
Dichloressigsaeure
UNII-9LSH52S3LQ
NSC-2654
EINECS 201-207-0
9LSH52S3LQ
DKhUK
UN1764
BRN 1098596
DTXSID2020428
CHEBI:36386
AI3-18370
DCA
MFCD00004223
DTXCID20428
DICHLOROACETIC ACID [MI]
Dichloroacetate, Potassium
DICHLOROACETIC ACID [HSDB]
DICHLOROACETIC ACID [IARC]
DICHLOROACETIC ACID [VANDF]
4-02-00-00498 (Beilstein Handbook Reference)
DICHLOROACETIC ACID [WHO-DD]
UN 1764
NCGC00091444-02
Kyselina dichloroctova (Czech)
2,2-Dichloroacetic Acid-2-13C
DICHLOROACETIC ACID (IARC)
CAS-79-43-6
SMR000059158
TF4
Acid, Bichloroacetic
Acid, Dichloroacetic
dicloroacetic acid
WLN: QVYGG
2,2-dichloro-acetic acid
SCHEMBL7777
MLS000028893
MLS001074861
MLS001424165
CHEMBL13960
NSC2654
BDBM227588
HMS2051P22
HMS2232H11
HMS3370D12
HMS3393P22
YGA47070
Dichloroacetic acid, puriss., 99%
Tox21_111133
Tox21_202363
Tox21_300419
Acetic acid, dichloro- (8CI,9CI)
BBL011449
LMFA01090070
MSK000808
STL146561
AKOS005720869
Tox21_111133_1
AT42091
CCG-101070
DB08809
NC00320
NCGC00091444-01
NCGC00091444-03
NCGC00091444-04
NCGC00167845-02
NCGC00254261-01
NCGC00259912-01
AS-14228
DB-056364
D0308
Dichloroacetic acid [UN1764] [Corrosive]
Dichloroacetic acid, biotech. grade, >=98%
NS00001485
Dichloroacetic acid, ReagentPlus(R), >=99%
EN300-20014
Q412845
DCA Deblock (0.36M dichloroacetic acid in toluene)
Dichloroacetic acid, PESTANAL(R), analytical standard
F2191-0226
Z104476414
Dichloroacetic acid 1000 microg/mL in Methyl-tert-butyl ether
5% Dichloroacetic Acid in Toluene (for AKTA oligopilottrade mark) NC-0406 emp Biotech GmbH
201-207-0
Solubility of 2,2-Dichloroacetic Acid
2,2-Dichloroacetic acid, with the chemical formula C2H2Cl2O2, is notable for its solubility characteristics in various solvents. This compound is primarily known for its polarity, which significantly influences its solubility. Here are some key points:
Overall, the solubility properties of 2,2-dichloroacetic acid are beneficial in chemical synthesis and various applications, highlighting its importance in the field of chemistry. As a compound, it exemplifies the relationship between polarity, molecular structure, and solubility behavior.