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22868-35-5

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22868-35-5 Usage

General Description

OTAVA-BB 1325766 is a chemical compound with a molecular formula of C20H18N4O4S2. It is a heterocyclic compound that contains both sulfur and nitrogen atoms in its structure. This chemical is a part of a class of compounds known as sulfonamides, which have been used in the development of various pharmaceuticals, including antibiotics and diuretics. The exact role and function of OTAVA-BB 1325766 have not been specified, but its chemical structure suggests that it may have potential pharmacological activities. Further research and testing are required to fully understand the properties and applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 22868-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22868-35:
(7*2)+(6*2)+(5*8)+(4*6)+(3*8)+(2*3)+(1*5)=125
125 % 10 = 5
So 22868-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClN2/c14-10-5-3-4-9(8-10)13-15-11-6-1-2-7-12(11)16-13/h1-8H,(H,15,16)

22868-35-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H64245)  2-(3-Chlorophenyl)benzimidazole, 95%   

  • 22868-35-5

  • 250mg

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H64245)  2-(3-Chlorophenyl)benzimidazole, 95%   

  • 22868-35-5

  • 1g

  • 2352.0CNY

  • Detail
  • Alfa Aesar

  • (H64245)  2-(3-Chlorophenyl)benzimidazole, 95%   

  • 22868-35-5

  • 5g

  • 9408.0CNY

  • Detail

22868-35-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-chlorophenyl)benzimidazole

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:22868-35-5 SDS

22868-35-5Relevant articles and documents

Synthesis of 2-substituted benzimidazoles in the presence of polyaniline nanoparticles doped with 12-tungstophosphoric acid as reusable heterogeneous catalyst

Abdollahi-Alibeik, Mohammad,Moosavifard, Marzieh,Poorirani, Safoora

, p. 1365 - 1371 (2013)

Polyaniline nanoparticles doped with 12-tungstophosphoric acid was prepared with different loading amounts of 12-tungstophosphoric acid. Doped polyaniline was characterized by XRD, SEM, and FT-IR techniques and the Keggin anion of heteropoly acid was dete

Nickel catalyzed sustainable synthesis of benzazoles and purines: Via acceptorless dehydrogenative coupling and borrowing hydrogen approach

Chakraborty, Gargi,Guin, Amit Kumar,Mondal, Rakesh,Paul, Nanda

, p. 7217 - 7233 (2021/08/30)

Herein we report nickel-catalyzed sustainable synthesis of a few chosen five-membered fused nitrogen heterocycles such as benzimidazole, purine, benzothiazole, and benzoxazole via acceptorless dehydrogenative functionalization of alcohols. Using a bench stable, easy to prepare, and inexpensive Ni(ii)-catalyst, [Ni(MeTAA)] (1a), featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA)), a wide variety of polysubstituted benzimidazole, purine, benzothiazole, and benzoxazole derivatives were prepared via dehydrogenative coupling of alcohols with 1,2-diaminobenzene, 4,5-diaminopyrimidine, 2-aminothiphenol, and 2-aminophenol, respectively. A wide array of benzimidazoles were also prepared via a borrowing hydrogen approach involving alcohols as hydrogen donors and 2-nitroanilines as hydrogen acceptors. A few control experiments were performed to understand the reaction mechanism.

Bandgap engineering in benzotrithiophene-based conjugated microporous polymers: a strategy for screening metal-free heterogeneous photocatalysts

Han, Songjie,Li, Ziping,Ma, Si,Zhi, Yongfeng,Xia, Hong,Chen, Xiong,Liu, Xiaoming

supporting information, p. 3333 - 3340 (2021/02/26)

Metal-free conjugated microporous polymers (CMPs) as visible-light active and recyclable photocatalysts offer a green and sustainable alternative to classical metal-based photosensitizers. However, the strategy for screening CMP-based heterogeneous photocatalysts has not been interpreted up to now. Herein, we present a general strategy for obtaining excellent solid photocatalysts, which is to implement bandgap engineering in the same series of materials. As a proof of concept, three conjugated porous materials containing benzo[1,2-b:3,4-b′:5,6-b′′]trithiophene building blocks (BTT-CMP1, BTT-CMP2 and BTT-CMP3) were successfully constructed. They possess permanent porosity with a large specific surface area and excellent stability. By changing the linker between benzotrithiophene units, the bandgaps, energy levels and photoelectric performances including the absorption, transient photocurrent responses and photocatalytic performances of BTT-CMPs could be handily modulated. Indeed, BTT-CMP2 displayed the best catalytic activity for visible-light-induced synthesis of benzimidazoles among the three CMP materials, even higher than that of small molecule photocatalysts. As a metal-free photocatalyst, interestingly, the screened BTT-CMP2 also showed extensive substrate applicability and outstanding recyclability. Additionally, we have the opinion that this strategy will prove to be a guiding principle for screening superior CMP-based photocatalysts and broaden their application fields.

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