Interesting facts
Interesting Facts About 5-Butylpyridine-2-carboxylic Acid
5-Butylpyridine-2-carboxylic acid is a fascinating organic compound that belongs to the pyridine family. Here are some compelling insights into this unique compound:
- Structural Complexity: The compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. This gives 5-butylpyridine-2-carboxylic acid distinctive chemical properties that are often leveraged in synthetic organic chemistry.
- Versatile Applications: This compound has potential applications in pharmaceuticals and the development of agrochemicals. Its carboxylic acid functionality can serve as a valuable precursor for more complex molecular constructions.
- Biological Significance: Compounds related to the pyridine structure have been investigated for their potential biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Understanding these effects could lead to novel therapeutic agents.
- Synthetic Pathways: The synthesis of 5-butylpyridine-2-carboxylic acid can involve various methods, such as functionalization of the pyridine ring. Organic chemists often explore new synthetic routes to enhance yields and reduce environmental impact.
- Chemical Reactivity: The presence of both the pyridine and carboxylic acid functionalities makes this compound a versatile building block in organic synthesis. Its ability to participate in nucleophilic substitution and other reactions can be a point of focus in research.
In the words of chemist Derek Lowe, "The beauty of organic synthesis lies not just in creating new compounds, but in the stories they tell through their reactivity and applications." 5-butylpyridine-2-carboxylic acid is a perfect example of this principle, making it an exciting topic of study for chemists and students alike.
Synonyms
fusaric acid
5-Butylpicolinic acid
536-69-6
5-Butylpyridine-2-carboxylic acid
Fusarinic acid
2-Pyridinecarboxylic acid, 5-butyl-
5-Butyl-2-pyridinecarboxylic acid
Picolinic acid, 5-butyl-
5-n-Butylpyridine-2-carboxylic acid
HSDB 3487
5-Butylpyridine-3-carboxylic acid
5-Butyl-pyridine-2-carboxylic acid
EINECS 208-643-0
MFCD00006298
NSC 19870
UNII-JWJ963070N
BRN 0125804
DTXSID5023085
JWJ963070N
NSC-19870
FUSARIC ACID [MI]
FUSARIC ACID [JAN]
FUSARIC ACID [HSDB]
CHEMBL24510
FUSARIC ACID [MART.]
CHEBI:5199
DTXCID703085
5-22-02-00384 (Beilstein Handbook Reference)
NSC19870
TNP00268
NCGC00015441-04
CAS-536-69-6
5-Butyl-pyridine-2-carboxylic acid (fusaric acid)
FUSARIC ACID (MART.)
Acid, Fusaric
5-Butyl-2-pyridinedicarboxylic Acid
5-Butylpicolinate
Prestwick_233
5 Butyl 2 pyridinedicarboxylic Acid
Acid, 5-Butyl-2-pyridinedicarboxylic
5-n-butylpicolinic acid
Prestwick0_000442
Prestwick1_000442
Prestwick2_000442
Prestwick3_000442
5-n-butyl picolinic acid
Lopac-F-6513
Lopac0_000526
Oprea1_115508
WLN: T6NJ BVQ E4
5-n-Butyl-2-picolinic acid
BSPBio_000484
MLS002153813
SCHEMBL178006
SPBio_002423
BPBio1_000534
Picolinic acid, 5-butyl-(8CI)
HMS1569I06
HMS2096I06
HMS2230M05
HMS3261J13
HMS3369P03
Tox21_110149
Tox21_500526
BDBM50000439
STL564384
AKOS015891748
CCG-204616
FF52452
Fusaric acid, from Gibberella fujikuroi
LP00526
SDCCGSBI-0050509.P002
NCGC00015441-01
NCGC00015441-02
NCGC00015441-03
NCGC00015441-05
NCGC00015441-06
NCGC00015441-07
NCGC00015441-08
NCGC00015441-10
NCGC00015441-15
NCGC00093919-01
NCGC00093919-02
NCGC00093919-03
NCGC00261211-01
AS-57621
SMR001233184
DB-052375
HY-128483
CS-0099145
EU-0100526
F0227
NS00011724
F 6513
T72585
Q905703
SR-01000075634
SR-01000075634-1
BRD-K87049188-001-03-6
Fusaric acid, for HPLC derivatization, >=99.0% (HPLC)
Fusarinic acid, 2.5-Butylpicolinic acid, Piconlinic acid
CQV
Solubility of 5-butylpyridine-2-carboxylic acid
The solubility of 5-butylpyridine-2-carboxylic acid (C11H13NO2) in various solvents is influenced by its unique structure and functional groups. In general, this compound displays a range of solubility behaviors:
In summary, the solubility of 5-butylpyridine-2-carboxylic acid can be described as:
Understanding these solubility characteristics is critical for applications in synthesis and formulation incorporating this compound.