Interesting facts
Interesting Facts about 4-Aminobenzamidine
4-Aminobenzamidine is a fascinating compound with numerous applications and properties that pique the interest of chemists and researchers alike. Here are some intriguing aspects:
- Key Functional Groups: This compound features both an amine group and an amidine, which allows it to behave as a versatile building block in synthetic organic chemistry.
- Role as a Precursor: 4-Aminobenzamidine is utilized as a precursor in the synthesis of various pharmaceuticals and biologically active compounds, making it a valuable asset in medicinal chemistry.
- Enzyme Inhibition: The compound has been studied for its potential to inhibit certain enzymes, which can be beneficial in developing treatments for diseases such as cancer and hypertension.
- Structure Functions: The molecular structure, featuring a benzene ring, contributes to its stability and reactivity, which are essential in drug formulation processes.
- Research Applications: Scientists examine 4-Aminobenzamidine for its applications in diagnostics, particularly in developing probes to study enzyme activities.
As noted by researchers, "4-aminobenzamidine’s ability to mimic natural substrates makes it a focal point in studying enzyme mechanisms." This capability enhances its utility in pharmacology, making it an important compound in modern drug discovery.
With ongoing research, the full potential of 4-Aminobenzamidine continues to unfold, promising exciting developments in the fields of chemistry and medicine.
Synonyms
4-aminobenzamidine
p-Aminobenzamidine
3858-83-1
4-Aminobenzenecarboximidamide
4-aminobenzimidamide
Benzenecarboximidamide, 4-amino-
Benzamidine, p-amino-
EINECS 223-370-7
4-Amino-benzamidine
NSC 227928
BRN 0386209
63GK9KT599
NSC-227928
4-AMINOBENZENE-1-CARBOXIMIDAMIDE
CHEMBL124632
DTXSID30191899
para-aminobenzamidine
p-Aminobenzamidine (dihydrochloride)
UNII-63GK9KT599
Lopac-A-7148
Lopac0_000070
1329499-33-3
ABD
SCHEMBL150756
WPANETAWYGDRLL-UHFFFAOYSA-
DTXCID20114390
BBL007616
BDBM50092660
NSC227928
STK367857
AKOS005444850
Benzenecarboximidamide, 4-amino-(9CI)
CCG-204165
SDCCGSBI-0050058.P002
NCGC00015084-01
NCGC00015084-02
NCGC00015084-03
NCGC00015084-04
NCGC00015084-05
NCGC00162057-01
DA-17009
(6S)-Tetrahydro-L-biopterin-d3 Disulfate
CS-0165920
NS00030422
EN300-70197
AB00374717-08
4-aminobenzimidamide? (Dabigatran Impurity pound(c)
Q27263611
InChI=1/C7H9N3/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H3,9,10)
223-370-7
Solubility of 4-Aminobenzamidine (C7H9N3)
The solubility characteristics of 4-aminobenzamidine can be quite fascinating. This compound belongs to the class of amidines, which generally exhibits interesting solubility behavior due to their polar functional groups.
Key Points on Solubility:
As a general rule, the solubility of amidines in water and organic solvents can be substantial, and understanding the solubility profile of 4-aminobenzamidine is crucial for applications in biological systems and pharmaceuticals. Furthermore, precise conditions in laboratory settings can be tailored to achieve optimal solubility for experimental needs.