Interesting facts
Interesting Facts About Benzamidine
Benzamidine is a fascinating compound known for its unique properties and diverse applications in various scientific fields. Here are some compelling facts about this interesting amide derivative:
- Chemical Nature: Benzamidine is classified as an aminobenzamide, featuring both an aromatic ring and an amidine functional group. This structural combination lends itself to unique chemical reactivities.
- Biological Significance: One of the most notable aspects of benzamidine is its role as a potent inhibitor of serine proteases, leading to its use in studies of blood coagulation and cellular functions. This has made it invaluable in biochemical research.
- Pharmaceutical Applications: Research has shown that benzamidine and its derivatives can exhibit pharmacological activities, including antiviral and antitumor properties. This potential opens doors to new therapeutic agents.
- Synthesis: Production of benzamidine can be achieved through various synthetic routes, including the reaction of benzoyl chloride with guanidine, demonstrating its accessibility for further studies and applications.
- Recognized in Scientific Literature: Benzamidine has made its mark in numerous publications, highlighting its effectiveness in enzymatic assays and other chemical investigations. It is often cited for its versatility in diverse research areas.
As a versatile compound, benzamidine serves as an excellent example of how simple molecular modifications can yield powerful biological tools. With ongoing research, it continues to reveal its potential in the scientific community, making it a compound worthy of attention.
Synonyms
benzamidine
618-39-3
Benzenecarboximidamide
Benzimidamide
Phenylamidine
CCRIS 2952
NSC 243704
UNII-KUE3ZY3J1F
KUE3ZY3J1F
EINECS 210-546-3
Benzenecarboxamidine
MFCD00042826
CHEBI:41033
Benzamidine (Protonated)
NSC-243704
CHEMBL20936
DTXSID8045012
Benzamidinium chloride
123920-06-9
BEN
.beta.-allo-2-Octulopyranose, 2,7-anhydro-1,4,8-trideoxy-5-O-(phenylmethyl)-
Benzenylamidine; NSC 243704; Phenylamidine;
1bra
1oss
2ast
benzene, amidino-
1c5o
1c5p
1c5z
1ce5
1f5k
1h4w
1v2j
1v2l
1v2m
1v2s
1v2u
1v2v
2j9n
Lopac-B-6506
SCHEMBL9207
Lopac0_000203
MLS001066369
GTPL7566
DTXCID6025012
1j14
1j15
1j16
1w80
HMS2233B11
HMS3370L08
ALBB-021313
BBL012141
BDBM50038002
NSC243704
STL163510
AKOS000201384
AB01943
BS-3750
CCG-204298
FB35345
SDCCGSBI-0050191.P002
NCGC00015160-01
NCGC00015160-02
NCGC00015160-03
NCGC00015160-04
NCGC00015160-05
NCGC00015160-07
NCGC00162090-01
SMR000471900
SY096666
DB-031147
CS-0103011
NS00000060
B10051
C01784
AB00691669-14
AE-641/30119009
Q4890748
64F5C29D-34E7-4815-B5F3-CC94EA3D2CAD
F1905-7123
125772-71-6
Solubility of Benzamidine
Benzamidine, with the chemical formula C7H8N2, exhibits noteworthy solubility characteristics that reflect its chemical nature. This compound is primarily soluble in polar solvents due to the presence of its amine group. Here are some key points to consider regarding its solubility:
Overall, benzamidine's solubility is influenced by its structure and the chemical environment, making it an interesting compound for various applications. As a rule of thumb, "like dissolves like," so the polar nature of benzamidine aids in its compatibility with polar solvents