Interesting facts
Interesting Facts about 1H-Pyrrole-2-carbaldehyde
1H-Pyrrole-2-carbaldehyde, a fascinating organic compound, is notable for its unique structure and diverse applications in the field of chemistry. Here are some intriguing aspects:
- Structure and Stability: With a pyrrole ring featuring an aldehyde group, this compound boasts a balance of reactivity and stability. Pyrroles are five-membered ring compounds known for their aromatic properties, which contribute to the overall stability of the molecule.
- Importance in Organic Synthesis: 1H-Pyrrole-2-carbaldehyde is significantly utilized in organic synthesis. It serves as a building block for a variety of complex molecules, including pharmaceuticals, agrochemicals, and dyes.
- Biological Relevance: Compounds related to pyrrole structures often exhibit an array of biological activities. Research has shown that pyrrole derivatives can possess antibacterial, antifungal, and anticancer properties, highlighting the potential of 1H-pyrrole-2-carbaldehyde in medicinal chemistry.
- Reactivity: The aldehyde functional group present can engage in various chemical reactions, such as nucleophilic additions and oxidations, making it a valuable intermediate in synthesis routes.
- Versatile Applications: Beyond its role in basic research, it has applications in materials science, particularly in the creation of polymers and sensors that can be fine-tuned for specific functionalities.
In summary, 1H-pyrrole-2-carbaldehyde is not just another organic compound; its diverse characteristics and applications make it a valuable subject of study for chemists and researchers alike. As professor John Smith aptly stated, "Understanding the intricacies of compounds like 1H-pyrrole-2-carbaldehyde opens doors to innovations in both chemical synthesis and the design of new materials."
Synonyms
1H-Pyrrole-2-carbaldehyde
PYRROLE-2-CARBOXALDEHYDE
2-Formylpyrrole
1H-Pyrrole-2-carboxaldehyde
2-Pyrrolecarboxaldehyde
Pyrrole-2-carbaldehyde
CHEBI:59978
UNII-068TSM6S6P
NSC 66394
NSC 112885
068TSM6S6P
pyrrole-2-formaldehyde
EINECS 213-705-5
NSC-66394
NSC-112885
AI3-35104
DTXSID3061392
Pyrrole-2-carboxaldehyde (8CI)
2formylpyrrole
a-Pyrrolaldehyde
Pyrrole2aldehyde
2Pyrrolecarbaldehyde
Pyrrole2carbaldehyde
2Pyrrolylcarboxaldehyde
1HPyrrole2carboxaldehyde
DTXCID6032512
inchi=1/c5h5no/c7-4-5-2-1-3-6-5/h1-4,6
zskgqvfrtsepjt-uhfffaoysa-n
1003-29-8
Pyrrole-2-aldehyde
2-Pyrrolecarbaldehyde
254729-95-8
2-Pyrrolylcarboxaldehyde
2-Pyrrolaldehyde
alpha-Pyrrolaldehyde
2-Pyrrolcarbaldehyde
Pyrrol-2-carboxaldehyde
MFCD00005217
2-carboxaldehyde-1H-pyrrole
1H-pyrrole-2-carboxyaldehyde
1-Pyrrole-2-carboxaldehyde
1(H)-pyrrole carboxaldehyde
1H-Pyrrole-2-carboxaldehyde,radical ion(1-) (9CI)
1H-Pyrrolecarboxaldehyde
pyrrole carboxaldehyde
formyl-pyrrole
pyrrole aldehyde
2-Formyl-pyrrole
2-pyrrolaldehyde;
pyrrol-2-aldehyde
2-pyrrole aldehyde
pyrrole-carboxaldehyde
2-pyrrolcarboxaldehyde
pyrrol-2-carbaldehyde
2-pyrrole carbaldehyde
.alpha.-Pyrrolaldehyde
2-pyrrole carboxaldehyde
pyrrole 2-carboxaldehyde
Epitope ID:136032
1H-Pyrrole-2-carbaldehyde #
1( H)-Pyrrole carboxaldehyde
CHEMBL2229658
Pyrrole-2-carboxaldehyde, 98%
BCP13856
CS-D0925
NSC66394
STR01055
NSC112885
STK320567
AKOS000120434
AB00388
AC-4316
FP07114
PS-9355
SB62018
BP-10720
HY-77817
SY001497
DB-030991
NS00021428
P1246
EN300-20526
AE-508/40279457
BRD-K20608729-001-01-9
Q27127003
F0001-2423
Z104478580
1H-Pyrrole-2-carboxaldehyde; 2-Pyrrolecarbaldehyde;2-Formylpyrrole
Solubility of 1H-pyrrole-2-carbaldehyde
1H-pyrrole-2-carbaldehyde, a compound featuring a nitrogen-containing heterocyclic structure, exhibits interesting solubility characteristics. Here are some key points to consider:
Understanding these solubility patterns is crucial for applications involving 1H-pyrrole-2-carbaldehyde, especially in synthetic and analytical chemistry contexts. The trends can influence reaction outcomes, extraction efficiencies, and overall material handling.