Interesting facts
Interesting Facts about 2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile
2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile is a fascinating compound with notable structural and functional properties. Here are some key points that highlight its scientific significance:
- Flavonoid Analogue: This compound is related to flavonoids, a diverse group of plant compounds known for their antioxidant properties. Its structure includes a phenyl group adorned with multiple hydroxyl (-OH) groups that enhance its ability to scavenge free radicals.
- Versatile Applications: Due to its unique structure, this compound finds applications in various fields, including medicinal chemistry, where it can serve as a scaffold for the design of new pharmaceuticals.
- Biological Activity: Compounds with similar structures have demonstrated significant biological activities including anti-inflammatory and anticancer properties, making this compound a potential candidate for further research.
- Synthesis: The key to synthesizing this compound lies in its functional groups. Chemists can exploit reactions that involve the formation of carbon-nitrogen bonds, allowing for the creation of derivatives that may exhibit enhanced properties.
As with many chemical compounds, the study of 2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile opens avenues for research into its potential health benefits and industrial applications. Exploring its properties further could lead to groundbreaking discoveries in various fields of science.
Synonyms
Tyrphostin 25
Tyrphostin A25
118409-58-8
Tyrphostin-25
2-[(3,4,5-trihydroxyphenyl)methylidene]propanedinitrile
Propanedinitrile, 2-[(3,4,5-trihydroxyphenyl)methylene]-
AG-82
RG-50875
DTXSID4045216
2-(3,4,5-Trihydroxybenzylidene)malononitrile
NSC676484
NSC-676484
NCGC00016046-02
2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile
AG 82; RG50875; RG-50875;RG 50875;Tyrphostin A 25; Tyrphostin AG 82
Tyrphostin A 25
NSC 676484
(3,4,5-Trihydroxybenzylidene)malononitrile
(3,4,5-Trihydroxybenzylidene)-malononitrile
alpha-Cyano-(3,4,5-trihydroxy)cinnamonitrile
((3,4,5-Trihydroxyphenyl)methylene)propanedinitrile
Propanedinitrile,2-[(3,4,5-trihydroxyphenyl)methylene]-
(4,5-Trihydroxybenzylidene)malononitrile
BiomolKI_000012
Lopac-T-7290
BiomolKI2_000022
Lopac0_001190
SCHEMBL239879
BDBM4341
BMK1-B12
C878BF87UY
CHEMBL310798
DTXCID2025216
Propanedinitrile, ((3,4,5-trihydroxyphenyl)methylene)-
CHEBI:92063
Tox21_110288
HSCI1_000114
MFCD00133900
AKOS040744891
CCG-100616
SDCCGSBI-0051157.P002
NCGC00016046-01
NCGC00016046-03
NCGC00016046-04
NCGC00016046-05
NCGC00094443-01
NCGC00094443-02
NCGC00094443-03
benzylidenemalononitrile (BMN) deriv. 25
DA-69079
TS-08179
HY-101958
CAS-118409-58-8
CS-0022227
EU-0101190
2-(3,4,5-Trihydroxybenzylidine)malononitrile
T 7290
SR-01000076172
AG 82 - CAS 118409-58-8
SR-01000076172-1
BRD-K03670461-001-03-8
Q27163858
Solubility of 2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile
The solubility of the compound 2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile, with the chemical formula C10H10O4, can be quite intriguing due to its complex structure.
In general, the solubility of organic compounds like this one may depend on several factors:
As a general note, it is observed that compounds with more hydrophilic groups tend to have higher solubility in water, while less polar or more hydrophobic structures can precipitate out, particularly in nonpolar solvents.
In summary: One might expect that 2-[(3,4,5-trihydroxyphenyl)methylene]propanedinitrile would exhibit reasonable solubility in polar solvents, especially considering its multiple hydroxyl functional groups, which provide both increased polar character and sites for hydrogen bonding.