Interesting facts
Interesting Facts about 3,6-Dichloropyridine-2-carboxylic Acid
3,6-Dichloropyridine-2-carboxylic acid is an intriguing compound that belongs to the class of pyridine derivatives. Here are some engaging facts about this compound:
- Structure: The presence of both chlorine atoms and a carboxylic acid group in its structure makes it a significant compound in various chemical applications. The dichloro substitutions can enhance its reactivity and interaction with other chemical species.
- Synthesis: This compound can be synthesized through several methods, including chlorination reactions, making it an attractive target for synthetic chemists interested in expanding their repertoire of useful intermediates.
- Biological Relevance: Compounds related to dichloropyridines have been researched for their biological activity, particularly in the fields of pharmaceuticals and agrochemicals. They often exhibit a range of activities, from antimicrobial to herbicidal properties.
- Versatile Intermediate: 3,6-Dichloropyridine-2-carboxylic acid serves as a versatile intermediate for developing other complex molecules, including potential drug candidates and agrochemicals.
- Environmental Concerns: With the increasing emphasis on environmental safety, studying the degradation and impact of such chlorinated compounds is crucial. Understanding their behavior in ecological systems is necessary for responsible application.
- Scientific Research: Researchers frequently investigate derivatives of this compound to unlock new pathways in medicinal chemistry. Innovations in drug design often hinge on modifying existing structures to enhance efficacy and reduce side effects.
"The pathway to discovery is often paved with derivatives and modifications of existing compounds," a common motto in the field of synthetic organic chemistry.
This compound, though it may seem niche, illustrates the *integral connection between chemical structure and biological function*, highlighting the critical balance that chemists strive to achieve in synthetic design.
Synonyms
CLOPYRALID
1702-17-6
3,6-Dichloropyridine-2-carboxylic acid
3,6-Dichloropicolinic acid
3,6-Dichloro-2-pyridinecarboxylic acid
2-Pyridinecarboxylic acid, 3,6-dichloro-
Clopyralide
Benzalox
Cirtoxin
Cyronal
Dowco 290
Acide dichloro-3,6 picolinique
Acide 3,6-dichloropicolinique
Acide 3,6-dichloropicolinique [French]
10G14M0WDH
Acide dichloro-3,6 picolinique [French]
DTXSID9029221
CHEBI:62961
CLOPYRALID [MI]
CLOPYRALID [ISO]
CLOPYRALID [HSDB]
DTXCID309221
3,6-DCP
Acide dichloro-3,6 picolinique (French)
3,6-Dichloro-2-Pyridinecarboxylicacid
3,6Dichloropicolinic acid
Acide 3,6dichloropicolinique
Picolinic acid, 3,6dichloro
Kyselina 3,6dichlorpikolinova
Acide dichloro3,6 picolinique
3,6Dichloro2pyridinecarboxylic acid
2Pyridine carboxylic acid, 3,6dichloro
USEPA/OPP Pesticide Code: 117403
2-Pyridinecarboxylic acid, 3,6-dichloro
3,6-Dichloro-2-pyridinecarboxylic acid, 3,6-Dichloropicolinic acid
216-935-4
Matrigon
Versatill
Format
Shield
Lontrel L
Lontrel 3
Lontrel 100
Lontrel 300
IWD 3523
XRM 3972
Kyselina 3,6-dichlorpikolinova
Picolinic acid, 3,6-dichloro-
MFCD00078655
Clopyralid 10 microg/mL in Acetonitrile
Campaign
Cliophar
Huiloralid
Clopyralid 100 microg/mL in Acetonitrile
Loncid
Crusader S
Lontrel SF 100
Caswell No. 323H
3,6-Dichloro-pyridine-2-carboxylic acid
CAS-1702-17-6
Clopyralid [ANSI:BSI:ISO]
HSDB 6593
EINECS 216-935-4
EPA Pesticide Chemical Code 117401
BRN 0473755
Kyselina 3,6-dichlorpikolinova [Czech]
UNII-10G14M0WDH
Clopiralid
2-Pyridine carboxylic acid, 3,6-dichloro-
Clopyralid (Standard)
SCHEMBL54779
5-22-02-00046 (Beilstein Handbook Reference)
CHEMBL1650605
HY-W018749R
Tox21_201435
Tox21_300876
3,6-dichloropyridine carboxylic acid
AC-330
STK373127
AKOS001083806
AB03013
CS-W019535
HY-W018749
PS-6031
3,6 Dichloropyridine-2-carboxylic acid
3,6-dichloro-2-pyridine carboxylic acid
NCGC00163834-01
NCGC00163834-02
NCGC00163834-04
NCGC00163834-05
NCGC00163834-06
NCGC00254780-01
NCGC00258986-01
DB-022127
D4117
EU-0000162
NS00005373
Clopyralid, PESTANAL(R), analytical standard
EN300-08124
C18779
D67447
F11213
SR-01000389672
Q2188539
SR-01000389672-1
Z56846826
Solubility of 3,6-dichloropyridine-2-carboxylic acid
3,6-dichloropyridine-2-carboxylic acid, with the chemical formula C6H4Cl2N2O2, exhibits interesting solubility properties that are influenced by its functional groups and structural characteristics. This compound is a derivative of pyridine with two chlorine substituents and a carboxylic acid group, leading to the following solubility traits:
Overall, the solubility characteristics of 3,6-dichloropyridine-2-carboxylic acid provide important insights for its usage in various chemical syntheses and applications. This compound is notably more soluble in aqueous solutions at elevated pH due to the deprotonation of the carboxylic acid group, illustrating the intricate relationship between molecular structure and solubility behavior.