Interesting facts
Interesting Facts about 3-[3-(dimethylaminomethyleneamino)-2,4,6-triiodo-phenyl]propanoic acid
This intriguing compound is not only notable for its complex structure but also for its diverse applications in various fields. Here are some interesting aspects:
- Structure Complexity: The compound features multiple functional groups, which contribute to its unique reactivity and properties. The presence of both a carboxylic acid and a triiodophenyl group highlights the interplay between hydrophilicity and hydrophobicity.
- Medical Relevance: Due to its iodine content, the triiodo-phenyl moiety may offer potential uses in medical imaging techniques, particularly in nuclear medicine, where iodine isotopes are frequently utilized as tracers.
- Organic Synthesis: The amine functionalities within this compound can serve as nucleophiles in various organic reactions, making it a useful precursor in the synthesis of more complex organic molecules.
- Color Properties: Iodinated compounds often exhibit unique color characteristics, which can be manipulated for various analytical applications, such as UV-Vis spectroscopy, potentially allowing for the exploration of colorimetric detection methods.
- Pharmacological Potential: Given the presence of the dimethylaminomethylene group, this compound might exhibit interesting pharmacological properties. Many compounds featuring amines are known for their physiological activity, which invites further investigation into therapeutic applications.
In summary, 3-[3-(dimethylaminomethyleneamino)-2,4,6-triiodo-phenyl]propanoic acid is a fascinating example of how intricate chemical structures can lead to a wealth of potential applications and further research opportunities. As a budding chemist, exploring the implications of such compounds can pave the way for innovative discoveries!
Synonyms
Iopodic acid
IPODATE
Ipodic acid
5587-89-3
Bilimin acid
Oragrafin
Oragrafin Sodium
HSDB 3347
EINECS 226-992-7
Biloptin
BRN 2220636
F604ZKI910
IPODATE [VANDF]
IPODATE [MI]
IPODIC ACID [HSDB]
3-(3-(((Dimethylamino)methylene)amino)-2,4,6-triiodophenyl)propanoic acid
3-[[(dimethylamino)methylene]amino]-3-(2,4,6-triiodophenyl)propionic acid
IOPODIC ACID [MART.]
IOPODIC ACID [WHO-DD]
Bilopten
DTXSID0023167
CHEBI:81496
2,4,6-Triiodo-3-((dimethylaminomethylene)amino)hydrocinnamic acid
3-[3-(dimethylaminomethylideneamino)-2,4,6-triiodophenyl]propanoic acid
beta-(3-(Dimethylaminomethyleneamino)-2,4,6-triiodophenyl)propionic acid
Biloptinon
3-(3-{[(E)-(dimethylamino)methylidene]amino}-2,4,6-triiodophenyl)propanoic acid
3-(((Dimethylamino)methylene)amino)-3-(2,4,6-triiodophenyl)propionic acid
IOPODIC ACID (MART.)
Sodium triiodohydrocinnamate
3-(3-{[(dimethylamino)methylidene]amino}-2,4,6-triiodophenyl)propanoic acid
ZK 15
NSC106962
SH 514
NCGC00181092-01
SQ 15761
SQ 15,761
iopodic-acid
UNII-F604ZKI910
3-(3-(((dimethylamino)methylidene)amino)-2,4,6-triiodophenyl)propanoic acid
Benzenepropanoic acid, 3-(((dimethylamino)methylene)amino)-2,4,6-triiodo-
1221-56-3
3-(3-Dimethylaminomethyleneamino-2,4,6-triiodophenyl)propionic acid
Hydrocinnamic acid, 3-(((dimethylamino)methylene)amino)-2,4,6-triiodo-
SCHEMBL37851
MLS004774078
DTXCID103167
CHEMBL1201243
CHEMBL3306201
2,4,6-TRIIODO-3-
YQNFBOJPTAXAKV-UHFFFAOYSA-N
BBL023886
STL069541
AKOS005689228
DB09333
SMR003500747
NS00007834
C18093
SBI-0653894.0001
EN300-25597632
BRD-K51956333-001-03-8
Q22294025
3-(3-(((Dimethylamino)methylene)amino)-2,4,6-triiodophenyl)propanoicacid
3-[3-[(E)-dimethylaminomethyleneamino]-2,4,6-triiodo-phenyl]propanoic acid
3-(3-{[(1E)-(dimethylamino)methylidene]amino}-2,4,6-triiodophenyl)propanoic acid
Solubility of 3-[3-(dimethylaminomethyleneamino)-2,4,6-triiodo-phenyl]propanoic acid
The solubility of 3-[3-(dimethylaminomethyleneamino)-2,4,6-triiodo-phenyl]propanoic acid can be quite intriguing given its complex structure. This compound exhibits unique characteristics that influence its solubility profile:
In conclusion, understanding the solubility of 3-[3-(dimethylaminomethyleneamino)-2,4,6-triiodo-phenyl]propanoic acid requires considering both its amphipathic nature and the solvent environment. Overall, it may display limited solubility in aqueous media, while showing better compatibility with organic solvents that can adequately stabilize its molecular structure.