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6-methoxy-2,2-diphenyl-2H-chromene is a complex organic compound belonging to the class of chromones, characterized by a benzopyran structure. It features a 2H-chromene core, which is a type of chromone with a hydrogen atom at the 2-position. The molecule is further defined by the presence of a methoxy group (-OCH3) at the 6-position, which introduces an oxygen atom and a methyl group, enhancing its reactivity and solubility. Additionally, two phenyl rings (C6H5) are attached to the 2-position of the chromene nucleus, contributing to its stability and aromaticity. 6-methoxy-2,2-diphenyl-2H-chromene is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various biologically active molecules. Its unique structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical intermediates.

1488-61-5

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1488-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1488-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1488-61:
(6*1)+(5*4)+(4*8)+(3*8)+(2*6)+(1*1)=95
95 % 10 = 5
So 1488-61-5 is a valid CAS Registry Number.

1488-61-5Downstream Products

1488-61-5Relevant academic research and scientific papers

Facile access to 2,2-diaryl 2: H -chromenes through a palladium-catalyzed cascade reaction of ortho -vinyl bromobenzenes with N -tosylhydrazones

Huang, Xueliang,Yu, Yinghua,Zhang, Heng

supporting information, p. 5115 - 5119 (2020/07/23)

A palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones has been developed, which provides a facile approach to 2,2-disubstituted 2H-chromenes. The migration of palladium from the aryl to vinyl position is crucial, as the in situ produced vinyl palladium intermediate could further react with diazo compounds to generate the reactive species for the sequential annulation. This journal is

Catalysis by β-Cyclodextrin Hydrate - Synthesis of 2,2-Disubstituted 2H-Chromenes in Aqueous Medium

Ghatak, Avishek,Khan, Sagar,Bhar, Sanjay

supporting information, p. 435 - 443 (2016/02/18)

A cost-effective, operationally simple and eco-compatible protocol for the one-pot synthesis of photochromic pyrans by the reaction of propargyl alcohols as well as propargyl ethers with differently substituted phenols under ambient atmosphere in aqueous

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