Interesting facts
Interesting Facts about 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine
This compound, 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine, is an intriguing molecule that falls under the class of hydrazones and amidines. Its structural complexity opens up many fascinating avenues for research and application:
- Biological Activity: This compound has been studied for its potential biological applications, particularly in the field of medicinal chemistry. It has shown properties that may be useful in the development of new pharmaceuticals.
- Enzyme Inhibition: The amidine functional group is known to interact with various enzymes. Compounds similar to this one have been investigated for their ability to inhibit specific enzymes, making them valuable for drug design.
- Synthesis Routes: The synthesis of 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine involves multiple synthetic steps that highlight the artistry of organic chemistry, particularly in manipulating functional groups to achieve desired reactivity.
- Structure-Activity Relationship (SAR): Researchers often explore SAR in compounds like this to understand how slight modifications can affect biological activity. It gives insight into the field of drug discovery.
- Versatility: Amidines have versatile reactivity profiles. They can serve as precursors for various synthetic transformations, leading to advanced materials and other functional compounds.
In summary, 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine represents a fascinating intersection of unique chemical structure and potential applications. As researchers continue to explore its properties, it may pave the way for new therapeutic agents and broaden our understanding of hydrazone chemistry.
Synonyms
DIMINAZENE
536-71-0
berenil
Diminazeno
Diminazenum
4,4'-(Diazoamino)benzamidine
DIMINAZEN
Pirocide
Diminazene [INN:BAN]
Diminazenum [INN-Latin]
Diminazene [INN]
Diminazeno [INN-Spanish]
Azidin
Diminazene [WHO-DD]
4,4'-(1-Triazene-1,3-diyl)bis-benzenecarboximidamide
CHEBI:81724
UNII-Y5G36EEA5Z
4-[2-(4-carbamimidoylphenyl)iminohydrazinyl]benzenecarboximidamide
EINECS 208-644-6
Y5G36EEA5Z
Benzenecarboximidamide, 4,4'-(1-triazene-1,3-diyl)bis-
4,4'-(1-Triazene-1,3-diyl)bis[benzenecarboximidamide]
DTXSID7043792
4,4'-(Triaz-1-ene-1,3-diyl)dibenzimidamide
Beronal
Bevenil
1443105-71-2
Diminazine
4-(2-(4-Carbamimidoylphenyl)iminohydrazinyl)benzenecarboximidamide
Diminazenum (INN-Latin)
Diminazeno (INN-Spanish)
4,4'-triaz-1-ene-1,3-diyldibenzenecarboximidamide
4,4'-Diazoaminobenzamidine
BRN
NSC114835
4,4' Diazoaminobenzamidine
4-((2E)-3-(4-carbamimidoylphenyl)triaz-2-en-1-yl)benzene-1-carboximidamide
4-[(2E)-3-(4-carbamimidoylphenyl)triaz-2-en-1-yl]benzene-1-carboximidamide
diminazene-aceturate
4,4'-(1-Triazene-1,3-diyl)bisbenzenecarboximidamide Dihydrochloride; 4,4'-(Diazoamino)dibenzamidine Dihydrochloride; Berenil Dihydrochloride;
MFCD00866606
Berenil (aceturate 2:1)
Diminazene [INN:WHO-DD]
CHEMBL35241
SCHEMBL120719
4,4'-(1-Triazene-1,3-diyl)bisbenzenecarboximidamide
DTXCID5023792
GTPL10307
XNYZHCFCZNMTFY-UHFFFAOYSA-N
GLXC-25308
BCP13959
BDBM50000999
RB8007
AKOS015895569
DB03608
HY-W342283
AC-22588
AS-75445
CS-0453371
NS00011721
C18388
AB01563384_01
AB01563384_02
Q410958
BRD-K92848252-001-01-9
BRD-K92848252-001-02-7
BRD-K92848252-001-03-5
4-[(2E)-2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine
DIMINAZINE ACETURATE; 1,3-TRIS-(4'AMIDINOPHENYL)TRIAZINE
4-[(1E)-3-(4-carbamimidoylphenyl)triaz-1-en-1-yl]benzenecarboximidamide
208-644-6
Solubility of 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine (C14H15N7)
The solubility of 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine is a nuanced topic, as it is influenced by various factors including temperature, pH, and the presence of solvents. This compound exhibits moderate to low solubility in aqueous solutions. Here’s what you need to know:
In summary, while 4-[2-(4-carbamimidoylphenyl)iminohydrazino]benzamidine may present challenges in solubility, understanding its interactions with different environments offers avenues for enhancing its bioavailability and applications in research and pharmaceutical development.