21547-71-7 Usage
Uses
Used in Pharmaceutical Research:
2-(1 H-BENZOIMIDAZOL-2-YLSULFANYL)-BUTYRIC ACID is used as a potential therapeutic agent for various medical conditions due to its unique chemical structure and properties. It is particularly of interest for the treatment of conditions such as cancer, inflammation, and neurological disorders.
Used in Cancer Treatment Research:
In the field of oncology, 2-(1 H-BENZOIMIDAZOL-2-YLSULFANYL)-BUTYRIC ACID is used as a research compound to explore its potential as an anticancer agent. Its specific interactions with biological targets and mechanisms of action are under investigation to determine its efficacy and safety in treating different types of cancer.
Used in Inflammation Management Research:
2-(1 H-BENZOIMIDAZOL-2-YLSULFANYL)-BUTYRIC ACID is also used in research aimed at managing inflammation. Its effects on inflammatory pathways and its potential to reduce inflammation-related symptoms are being studied.
Used in Neurological Disorders Research:
In the context of neurological disorders, 2-(1 H-BENZOIMIDAZOL-2-YLSULFANYL)-BUTYRIC ACID is used as a research compound to investigate its potential to alleviate symptoms or slow the progression of certain neurological conditions.
Used in Experimental Applications:
2-(1 H-BENZOIMIDAZOL-2-YLSULFANYL)-BUTYRIC ACID is utilized in experimental settings to further understand its chemical behavior, interactions with biological systems, and its overall potential as a pharmaceutical drug. This includes testing its stability, solubility, and pharmacokinetics in various models.
Check Digit Verification of cas no
The CAS Registry Mumber 21547-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,4 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21547-71:
(7*2)+(6*1)+(5*5)+(4*4)+(3*7)+(2*7)+(1*1)=97
97 % 10 = 7
So 21547-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2S/c1-2-9(10(14)15)16-11-12-7-5-3-4-6-8(7)13-11/h3-6,9H,2H2,1H3,(H,12,13)(H,14,15)/p-1/t9-/m1/s1
21547-71-7Relevant academic research and scientific papers
Synthesis and Antimicrobial Activity of Some 2-Alkyl-2H-1,4-benzothiazin-3(4H)-ones and 2-Alkylbenzoimidazolo-thiazolidin-3-ones
Koos, M.
, p. 1011 - 1016 (2007/10/02)
Sodium 2-aminothiophenoxide (1) reacts with ethyl 2-bromoalkanoates (2) under direct cyclization to form 2-alkyl-2H-1,4-benzothiazin-3(4H)-ones (3).Reaction of the sodium salt of 2-mercaptobenzimidazole (4) with 2 or 2-bromoalkanoic acids (5) affords only S-alkylated products (6 or 7, respectively).The cyclization products - 2-alkylbenzoimidazolothiazolidin-3-ones (8) - can be obtained only from the corresponding 2-(2-benzimidazolylthio)alkanoic acids (7) by the action of acetic anhydride.Both compounds 3 and 8 exhibit only moderate antimicrobial activity against some gram-positive bacteria. - Keywords: 4H-1,4-Benzothiazines; Benzoimidazolothiazolidines; Antimicrobial activity.
1,3-thiazoles and their use as immunomodulators
-
, (2008/06/13)
Heterocyclic sulfides of the general formula heterocycle-S-R, a process for their preparation and, in particular, their use for immunostimulation, immunorestoration and cytostatic treatment, and pharmaceutical agents, which contain a sulfide of this type, for these indications.
