7469-00-3 Usage
Guanidine derivative
A compound derived from guanidine, which is an organic compound with the structure H2N-C(=NH)-NH2.
Organic synthesis
1,2-dinaphthalen-1-ylguanidine is used as a reagent in the synthesis of organic compounds, particularly heterocyclic compounds and coordination complexes.
Heterocyclic compounds
These are organic compounds containing a ring of atoms with at least one atom not being carbon, such as nitrogen, oxygen, or sulfur.
Coordination complexes
These are compounds consisting of a central metal atom or ion bonded to a certain number of molecules or ions, known as ligands, through coordinate covalent bonds.
Antifungal properties
1,2-dinaphthalen-1-ylguanidine exhibits antifungal activity, which means it can inhibit the growth of fungi.
Antibacterial properties
The compound also has antibacterial properties, indicating that it can inhibit the growth of bacteria.
Medicinal chemistry
1,2-dinaphthalen-1-ylguanidine has potential applications in medicinal chemistry, which is the study of chemical compounds that have biological activity and can be used as drugs.
Pharmacology
The study of the interactions between drugs and living systems, including their effects, mechanisms of action, and therapeutic uses.
Potential use in cancer treatment
1,2-dinaphthalen-1-ylguanidine has been studied for its potential use in the treatment of cancer, although further research is needed to fully understand its pharmacological properties and potential therapeutic uses.
Further research needed
More research is required to fully understand the compound's pharmacological properties, potential therapeutic uses, and any possible side effects or limitations.
Check Digit Verification of cas no
The CAS Registry Mumber 7469-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7469-00:
(6*7)+(5*4)+(4*6)+(3*9)+(2*0)+(1*0)=113
113 % 10 = 3
So 7469-00-3 is a valid CAS Registry Number.
7469-00-3Relevant articles and documents
Cleavage of C-N bonds in guanidine derivatives and its relevance to efficient C-N bonds formation
Chang, Denghu,Zhu, Dan,Zou, Peng,Shi, Lei
, p. 1684 - 1693 (2015/03/30)
Efficient nonenzymatic decomposition of guanidine derivatives with high structural and functional diversity into anilide products is achieved in the presence of PdII/Cu(II) carboxylates/CO, relying on a dual C-N bonds cleavage strategy. In this decomposition process, the cooperative action of PdII species, Cu(II) carboxylates, and CO provides not only the N-acylating agents but also an initiator to trigger this C-N bonds cleavage sequence. The current results indicate that PdII/Cu(II) carboxylates/CO system provides a convenient and practical method for highly selective cleavage of unreactive C-N single bonds.
Synthesis and Structure-Activity Studies of N,N'-Diarylguanidine Derivatives. N-(1-Naphthyl)-N'-(3-ethylphenyl)-N'-methylguanidine: A New, Selective Noncompetitive NMDA Receptor Antagonist
Reddy, N. Laxma,Hu, Lain-Yen,Cotter, Ronald E.,Fischer, James B.,Wong, Wen Jee,et al.
, p. 260 - 267 (2007/10/02)
Diarylguanidines, acting as NMDA receptor ion channel site ligands, represent a new class of potential neuroprotective drugs.Several diarylguanidines structurally related to N,N'-di-o-tolylguanidine (DTG), a known selective ? receptor ligand, were synthes
N,N'-disubstituted guanidines and their use as excitatory amino acid antagonists
-
, (2008/06/13)
Disubstituted guanidines, e.g., bis-1,3-(o-isopropylphenyl)guanidine, bis-1,3-(m-isopropylphenyl)guanidine, bis-1,3-(1-naphthyl)guanidine, bis-1,3-(m-methoxyphenyl)guanidine, N-(1-naphthyl)-N'-(o-iodophenyl)-guanidine, N-(1-naphthyl)-N'-(m-ethylphenyl)gua
