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4-(Di-thiophen-2-yl-methyl)-phenol is an organic compound with the chemical formula C15H12OS2. It is characterized by a phenol group (C6H5OH) with a di-thiophen-2-yl-methyl group attached at the 4-position. The di-thiophen-2-yl-methyl group consists of two thiophene rings (a five-membered ring with sulfur atoms) connected to a methyl group. 4-(DI-THIOPHEN-2-YL-METHYL)-PHENOL is known for its potential applications in the synthesis of various organic materials, such as polymers and dyes, due to its unique structure and properties. It is also of interest in the field of materials science for its potential use in the development of electronic and optoelectronic devices.

727-66-2

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727-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727-66-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 727-66:
(5*7)+(4*2)+(3*7)+(2*6)+(1*6)=82
82 % 10 = 2
So 727-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12OS2/c16-12-7-5-11(6-8-12)15(13-3-1-9-17-13)14-4-2-10-18-14/h1-10,15-16H

727-66-2Downstream Products

727-66-2Relevant academic research and scientific papers

Melamine trisulfonic acid: A new efficient catalyst for the synthesis of aryldithienylmethanes

Wu, Liqiang,Yan, Yunhui,Yan, Fulin

experimental part, p. 149 - 154 (2012/02/16)

An efficient method has been developed for the synthesis of dithienylmethanes via bisarylation of aldehydes with thiophene in the presence of melamine trisulfonic acid as a catalyst under solvent-free conditions.

Unique versatility of Amberlyst 15. An acid and solvent-free paradigm towards synthesis of bis(heterocyclyl)methane derivatives

Singh, Kamaljit,Sharma, Shivali,Sharma, Amit

scheme or table, p. 34 - 37 (2011/10/17)

Bis(heterocyclyl)methanes, key intermediates for a variety of chemical, biochemical and material science relevant targets, have been obtained in a synthetically useful manner using Amberlyst 15 ion-exchange resin. This method promises versatility, cost-ef

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