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1-(3-hydroxy-4-methoxybenzyl)-2-(3-hydroxy-4-methoxyphenyl)-1H-1,3-benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

346612-71-3

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346612-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346612-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,6,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 346612-71:
(8*3)+(7*4)+(6*6)+(5*6)+(4*1)+(3*2)+(2*7)+(1*1)=143
143 % 10 = 3
So 346612-71-3 is a valid CAS Registry Number.

346612-71-3Downstream Products

346612-71-3Relevant academic research and scientific papers

Practical, ecofriendly, and chemoselective method for the synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles using amberlite IR-120 as a reusable heterogeneous catalyst in aqueous media

Sharma, Saikat Das,Konwar, Dilip

, p. 980 - 991 (2009)

A simple, efficient, and environmentally benign method has been developed for the exclusive formation of biologically significant 2-aryl-1-arylmethyl-1H- benzimidazoles under the heterogeneous catalysis of Amberlite IR-120 in aqueous media in excellent yi

MWCNTs-ZrO2 as a reusable heterogeneous catalyst for the synthesis of N-heterocyclic scaffolds under green reaction medium

Halder, Bipasa,Banerjee, Flora,Nag, Ahindra

, (2020/07/24)

A simple, efficient, and facile heterogeneous multi-walled carbon nanotubes-zirconia nanocomposite (MWCNTs-ZrO2) has been synthesized using natural feedstock coconut juice (água-de-coco do Ceará). The synthesized catalyst was characterized by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, and X-ray photoelectron spectroscopy analysis. The heterogeneous nanocomposite has been used for one-pot synthesis of various N-heterocyclic compounds like pyrazoles, 1,2-disubstituted benzimidazoles, 2-arylbenzazoles, and 2,3-dihydroquinazolin-4(1H)-ones under green reaction medium at room temperature. This novel method has several advantages, such as short reaction time, simple work-up, excellent yield, and green reaction conditions. The catalyst was recycled up to four times without significant loss in catalytic activity.

A simple and straightforward synthesis of substituted 2-arylbenzimidazoles over silica gel

Chaturvedi, Amit K.,Negi, Arvind S.,Khare, Puja

, p. 4500 - 4504 (2013/04/24)

A solid phase strategy for the synthesis of substituted 2-arylbenzimidazoles over silica gel has been achieved starting from their corresponding o-phenylenediamines 1 and aromatic aldehydes 2. The reaction is very simple, convenient and straightforward, a

Selective synthesis of 2-aryl-1-benzylated-1H-benzimidazoles

Shaterian, Hamid Reza,Fahimi, Nafiseh,Azizi, Kobra

experimental part, p. 2389 - 2393 (2012/02/04)

An efficient and simple procedure was developed for the green synthesis of various 2-aryl-1-ben-zylated-1H-benzimidazoles in high yields by condensation of o-phenylenediamine with aldehydes with P2O5/SiO 2 as catalyst unde

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