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1H-Benzimidazole, 2-[2-(4-chlorophenyl)ethenyl]-, also known as 2-[2-(4-chlorophenyl)vinyl]-1H-benzimidazole, is an organic compound with the molecular formula C14H10ClN and a molecular weight of 229.69 g/mol. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The compound features a 4-chlorophenyl group attached to a vinyl group, which is further connected to the benzimidazole core. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antifungal agents and herbicides. Due to its potential applications in the development of new drugs and chemicals, it is an important compound in the field of medicinal chemistry and chemical research.

2562-87-0

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2562-87-0 Usage

Type of compound

Organic compound

Use

Proton pump inhibitor (reduces stomach acid production)

Treats conditions

Gastroesophageal reflux disease (GERD), peptic ulcers

Mechanism of action

Irreversibly binds to the H+/K+ ATPase enzyme system at the secretory surface of the gastric parietal cells

Administration

Orally (delayed-release capsules or tablets)

Physical properties

White to off-white crystalline powder, sparingly soluble in water

Importance

Considered an essential medicine by the World Health Organization for treating acid-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 2562-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2562-87:
(6*2)+(5*5)+(4*6)+(3*2)+(2*8)+(1*7)=90
90 % 10 = 0
So 2562-87-0 is a valid CAS Registry Number.

2562-87-0Relevant academic research and scientific papers

Green syntheses of n-alkyl-2-styrylbenzimidazoles

Kumar, T. Ashok,Devi, B. Rama,Dubey

, p. 9569 - 9572 (2014/01/06)

Simple and green methodologies for the syntheses of 2-styrylbenzimidazoles (3a-c) and its N-alkyl derivatives (7a-i) have been developed. o-Phenylenediamine (1) was condensed with cinnamic acids (2a-c) resulting in 2-styrylbenzimidazoles (3a-c) using glycerol as a green and efficient solvent. 3 were also prepared alternatively by the condensation of 2-methylbenzimidazole (4) with benzaldehydes (5a-c) using glycerol as solvent. 2-Styrylbenzimidazoles (3a-c) and 2-methylbenzimidazole (4) were alkylated independently to obtain N-alkyl- 2-styrylbenzimidazole (7a-i) and N-alkyl-2-methylbenzimidazole (6a-c), respectively using DMS/DES/PhCH2Cl applying green methods such as simple physical grinding of reactants in solid phase, treating reactants in PEG-600 as a solvent in solution phase and using microwave irradiation of reactants respectively. Compounds 7a-i could also be prepared, alternatively, by heating 6a-c with 5a-c in glycerol at 180 °C for 3-4 h.

Microwave-assisted solvent-free synthesis of some styryl dyes with benzimidazole nucleus

Wang, Lanying,Zhang, Xiaogang,Li, Fengmei,Zhang, Zuxun

, p. 2245 - 2252 (2007/10/03)

A series of styryl dyes: 2-substituted styryl benzimidazole and α-methyl-2-substituted styryl benzimidazole were synthesized under solvent-free microwave irradiation by the condensation of 2-methylbenzimidazole or 2-ethylbenzimidazole with aromatic aldehydes in the presence of Ac 2O.

Application of Phase-Transfer Catalysis to the Synthesis of Mono- and Bis-stilbenes and Styryls

Lokhande, S. B.,Rangnekar, D. W.

, p. 485 - 488 (2007/10/02)

A novel and convenient method has been developed for the synthesis of substituted stilbenes by the condensation of active methyl group in suitably substituted toluenes with aromatic aldehydes in aq. medium at room temperature using benzyltriethylammonium chloride as a phase-transfer catalyst.This method has also been applied for the preparation of heterocyclic styryls and extended to the synthesis of bis-stilbenes and bis-styryls using aromatic dialdehydes in place of monoaldehydes.A comparison of the results shows that the present method is superior to the conventional methods in many respects.

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