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1H-Benzimidazole, 2-[2-(4-methoxyphenyl)ethenyl]-, also known as 2-[2-(4-Methoxyphenyl)vinyl]-1H-benzimidazole, is an organic compound with the molecular formula C15H13N2O. 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-methoxyphenyl 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 development of compounds with potential therapeutic applications. Its unique structure and properties make it a valuable building block in the creation of new molecules with desired biological activities.

2562-89-2

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2562-89-2 Usage

Molecular weight

250.29 g/mol

Structure

Benzimidazole derivative with a substituted phenylethynyl group

Applications

a. Organic synthesis
b. Pharmaceutical research
c. Anti-cancer studies
d. Antiparasitic studies
e. Antiviral studies
f. Treatment of neurological disorders

Potential uses

a. Materials science
b. Building block for functional organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 2562-89-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 2562-89:
(6*2)+(5*5)+(4*6)+(3*2)+(2*8)+(1*9)=92
92 % 10 = 2
So 2562-89-2 is a valid CAS Registry Number.

2562-89-2Downstream Products

2562-89-2Relevant academic research and scientific papers

One-pot chemo/regio/stereoselective generation of a library of functionalized spiro-oxindoles/pyrrolizines/pyrrolidines from α-aroylidineketene dithioacetals

Dhanalakshmi, Pandi,Babu, Seenivasagaperumal Sriram,Thimmarayaperumal, Solaimalai,Shanmugam, Sivakumar

, p. 33705 - 33719 (2015)

An efficient chemo/regio/stereoselective synthesis of novel and functionalized spiro-oxindole/pyrrolizine/pyrrolidine scaffolds has been achieved. The in situ generated azomethine ylide from isatin & l-proline/phenyl alanine underwent 1,3-dipolar cycloadd

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.

2-Aryl-substituted benzo-anellated 5-membered heterocycles as potential effectors in the cardiovascular system. Part 2

Rose

, p. 775 - 777 (2007/10/02)

In the course of investigations on structure-activity relationships of fostedil-and sulmazole-analoguesly fused 5-membered heterocycles, 1,3-benzimidazoles were obtained by simple cyclisation. In vitro experiments on isolated organs demonstrate markedly positive inotropic effects of some derivatives, whereas others exert both relaxing activity on smooth musculature in vitro and antihypertensive effects in vivo. Moreover they exhibit fungicide properties in vitro.

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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