125252-52-0 Usage
Type of compound
Quaternary ammonium salt
1) Heptyl group (C7H15)
A hydrophobic alkyl chain with seven carbon atoms.
2) Indole core
A heterocyclic aromatic ring system with a pyrrole and a benzene ring fused together.
3) Methyl groups (C1H3)
Three methyl groups attached to the indole core, contributing to its hydrophobic nature.
4) Cationic head group
A positively charged nitrogen atom with bulky substituents.
5) Bromide ion (Br-)
A negatively charged halogen anion that balances the cationic charge.
1) Low melting point
Facilitates ease of handling and processing.
2) High thermal stability
Resistant to decomposition at high temperatures, making it suitable for various applications.
3) Good solubility in organic solvents
Allows for easy incorporation into various chemical systems and reactions.
1) Antimicrobial agent
Due to its ability to disrupt cell membranes and interact with biomolecules.
2) Solvent
Its unique properties make it suitable for dissolving a wide range of compounds.
3) Surfactant
The combination of hydrophilic and hydrophobic groups allows it to reduce surface tension in solutions.
4) Catalysis
As a phase transfer catalyst, it can facilitate reactions between different phases, improving reaction rates and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 125252-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125252-52:
(8*1)+(7*2)+(6*5)+(5*2)+(4*5)+(3*2)+(2*5)+(1*2)=100
100 % 10 = 0
So 125252-52-0 is a valid CAS Registry Number.
125252-52-0Relevant articles and documents
N-Alkylated 2,3,3-trimethylindolenines and 2-methylbenzothiazoles. Potential lead compounds in the fight against Saccharomyces cerevisiae infections Dedication in memory of the late Derek Bennett 17-07-1931 to 05-04-2013.
Tyler, Andrew R.,Okoh, Adeyi Okoh,Lawrence, Clare L.,Jones, Vicky C.,Moffatt, Colin,Smith, Robert B.
, p. 222 - 227 (2013)
The synthesis of a variety of N-alkylated 2,3,3-trimethylindolenines and 2-methylbenzothiazoles is reported herein. Their potential as antifungal agents is evaluated by preliminary screening against Saccharomyces cerevisiae (S. cerevisiae), Schizosaccharomyces pombe (S. pombe), and Candida albicans (C. albicans). Statistical analyses illustrate a strong relationship between chain length and growth inhibition for S. cerevisiae and S. pombe (p 0.0001 in every case). Of particular interest is the activity of both sets of compounds against S. cerevisiae, as this is emerging as an opportunistic pathogen, especially in immunosuppressed and immunocompromised patients. Bioassays were set up to compare the efficacy of our range of N-alkylated compounds against classic antifungal agents; Amphotericin B and Thiabendazole.
