245-58-9 Usage
Uses
As the specific applications of 2H-[1,3]Thiazino[3,2-a]benzimidazole(8CI,9CI) have not been extensively studied, its uses are currently speculative based on its structural features. However, given its potential pharmacological activity, it can be hypothesized that 2H-[1,3]Thiazino[3,2-a]benzimidazole(8CI,9CI) may find utility in various fields such as medicine, pharmaceuticals, and material sciences.
Used in Pharmaceutical Industry:
2H-[1,3]Thiazino[3,2-a]benzimidazole(8CI,9CI) could be used as a bioactive molecule for the development of new drugs, given its heterocyclic structure that may allow it to interact with biological targets.
Used in Medicinal Chemistry Research:
As a compound with potential pharmacological activity, 2H-[1,3]Thiazino[3,2-a]benzimidazole(8CI,9CI) may serve as a starting point for medicinal chemistry research aimed at discovering new therapeutic agents.
Used in Material Sciences:
Due to its unique structure, 2H-[1,3]Thiazino[3,2-a]benzimidazole(8CI,9CI) might also be explored for its potential applications in material sciences, such as in the development of new materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 245-58-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 245-58:
(5*2)+(4*4)+(3*5)+(2*5)+(1*8)=59
59 % 10 = 9
So 245-58-9 is a valid CAS Registry Number.
245-58-9Relevant academic research and scientific papers
Heterocyclizations of 2-allylthiobenzimidazoles under the action of bromine
Korotkikh,Raenko,Aslanov
, p. 610 - 618 (2007/10/03)
Heterocyclizations of 2-allylthiobenzimidazoles under the action of bromine yield 3-bromo-3,4-dihydro-2H-benzimidazo[2,1-b][1,3]thiazine and 2H- or 4H-benzimidazo[2,1-b][1,3]thiazines via intermediate formation of 2-(2,3-dibrompropylthio)benzimidazoles. P
Heterocyclization of 2-Allylthiobenzimidazoles into Derivatives of Benzimidazo-1,3-Thiazines
Korotkikh, N. I.,Raenko, G. F.,Shvaika, O. P.
, p. 359 - 363 (2007/10/03)
It was found that bromination of 2-allylthiobenzimidazoles in organic solvents forms products of addition of bromine to the olefin bond - 2,3-dibromopropylthiobenzimidazoles, whch spontaneously or on heating cyclize into 3-bromobenzimidazo-1,3-thiazines or cyclodehydrobromination products - 2H- or 4H-benzimidazo-1,3-thiazines.
REARRANGEMENT OF 1-(2-PROPYNYL)BENZIMIDAZOLINE-2-THIONES TO 2H(4H)-1,3-THIAZINOBENZIMIDAZOLES
Klyuev, N. A.,Krasovskii, A. N.,Sheinkman, A. K.,Krasovskii, I. A.,Zhil'nikov, V. G.
, p. 1555 - 1561 (2007/10/02)
1-(2-Propynyl)-2-chlorobenzimidazoles were synthesized by the reaction of 2-chlorobenzimidazoles with propargyl bromide.When boiled with thiourea, they are converted into 1-(2-propynyl)benzimidazolin-2-thiones.When heated in an alcohol solution of potassium hydroxide, the latter rearrange to mixtures of isomeric 2H(4H)-1,3-thiazinobenzimidazoles.
