10060-88-5 Usage
Uses
Used in Pharmaceutical Industry:
2-imino-alpha-phenylthiazolidin-3-ethanol is used as a potential therapeutic agent for its anti-inflammatory properties, making it a candidate for treating conditions characterized by inflammation. Its anti-ulcer activity suggests its use in the development of medications to treat gastrointestinal ulcers, while its anti-oxidant properties indicate potential applications in combating oxidative stress-related disorders.
Used in Environmental Applications:
As a chelating agent, 2-imino-alpha-phenylthiazolidin-3-ethanol is used for the sequestration of heavy metal ions, which can be beneficial in environmental remediation processes to mitigate the toxic effects of heavy metals in soil and water systems.
Used in Antimicrobial and Antifungal Applications:
2-imino-alpha-phenylthiazolidin-3-ethanol is utilized as an antimicrobial and antifungal agent, indicating its potential use in the development of new antibiotics and antifungal drugs to combat resistant strains and treat infections.
These applications highlight the versatility of 2-imino-alpha-phenylthiazolidin-3-ethanol across different fields, underscoring its importance in ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 10060-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,6 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10060-88:
(7*1)+(6*0)+(5*0)+(4*6)+(3*0)+(2*8)+(1*8)=55
55 % 10 = 5
So 10060-88-5 is a valid CAS Registry Number.
10060-88-5Relevant academic research and scientific papers
DIHYDRO-5,6 IMIDAZOTHIAZOLES, DIHYDRO-2,3 IMIDAZOBENZOTHIAZOLES, ANALOGUES DU LEVAMISOLE
Amarouch, H.,Loiseau, P. R.,Bonnafous, M.,Caujolle, R.,Payard, M.,et al.
, p. 421 - 438 (2007/10/02)
New compounds containing 5,6-dihydro imidazothiazole 2,3,5,6-tetrahydro imidazothiazole and 2,3-dihydro imidazobenzothiazole rings, substituted by heterocycles analogue to chromones, were synthesized and screened against three nematodes, in vitro.The results indicate moderate anthelmintic properties, compared to levamisole; nevertheless, some products exhibit a significant degree of activity.
