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2‐(hydroxymethyl)‐7,7‐dimethyl‐10‐phenyl‐7, 8‐dihydropyrano[3,2‐b]chromene‐4, 9(6H, 10H)‐dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1256451-54-3

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1256451-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256451-54-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,4,5 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1256451-54:
(9*1)+(8*2)+(7*5)+(6*6)+(5*4)+(4*5)+(3*1)+(2*5)+(1*4)=153
153 % 10 = 3
So 1256451-54-3 is a valid CAS Registry Number.

1256451-54-3Downstream Products

1256451-54-3Relevant academic research and scientific papers

Inhibition of tyrosinase by 4H-chromene analogs: Synthesis, kinetic studies, and computational analysis

Brasil, Edikarlos M.,Canavieira, Luciana M.,Cardoso, érica T. C.,Silva, Edilene O.,Lameira, Jer?nimo,Nascimento, José L. M.,Eifler-Lima, Vera L.,Macchi, Barbarella M.,Sriram, Dharmarajan,Bernhardt, Paul V.,Silva, José Rogério Araújo,Williams, Craig M.,Alves, Cláudio N.

, p. 804 - 810 (2017)

Inhibition of mushroom tyrosinase was observed with synthetic dihydropyrano[3,2-b]chromenediones. Among them, DHPC04 displayed the most potent tyrosinase inhibitory activity with a Ki value of 4?μm, comparable to the reference standard inhibitor kojic acid. A kinetic study suggested that these synthetic heterocyclic compounds behave as competitive inhibitors for the L-DOPA binding site of the enzyme. Furthermore, molecular modeling provided important insight into the mechanism of binding interactions with the tyrosinase copper active site.

Chloroaluminate ionic liquid-modified silica-coated magnetic nanoparticles: Efficient and reusable catalyst for selective synthesis of mono- and bis-dihydropyrano[3,2-b]chromenediones

Estakhri, Ehsan,Nasr-Esfahani, Mahboobeh,Mohammadpoor-Baltork, Iraj,Tangestaninejad, Shahram,Moghadam, Majid,Mirkhani, Valiallah

, (2017)

The synthesis, characterization and catalytic activity of chloroaluminate ionic liquid-modified silica-coated magnetic nanoparticles ([SiPrPy]AlCl4@MNPs) are described. The prepared magnetic nanocatalyst was characterized using Fourier transfor

Synthesis and Bioassay of Dihydropyrano[3,2-b]chromenediones

Chereddy, Syama Sundar,Nemallapudi, Bakthavatchala Reddy,Balam, Satheesh Krishna,Soora Harinath, Jaya Prakash,Chinthaparthi, Radha Rani,Cirandur, Suresh Reddy

, p. 493 - 498 (2016)

Ytterbium perfluorooctanoate [Yb(PFO)3] is found to be an efficient catalyst for the microwave-irradiated synthesis of dihydropyrano[3,2-b]chromenediones by the one-pot condensation of kojic acid, aldehydes, and 1,3-dicarbonyl compound under so

Nano-pistachio hull-O xTiCl4?x: synthesis, characterization and application as an effective and novel nanocatalyst for one-pot synthesis of dihydropyrano[3,2-b]chromenedione derivatives

Shafe-Mehrabadi, Sayed Rasul,Sadeghi, Bahareh,Mosslemin, Mohammad Hossein,Hashemian, Saeedeh

, p. 1137 - 1145 (2020/10/29)

According to the Food and Agriculture Organization (FAO), Iran is the largest pistachio (Pistacia vera) producer in the world. Nevertheless, pistachio by-products (PBs) contain a high level of phenolic and cellulose compounds, it can be used as a substrat

Anchoring of nickel (II) kojic acid in functionalized Si-MCM‐41 matrix: a effective nanocatalyst for the catalytic clean synthesis of dihydropyrano[3,2-b]chromenediones

Noroozi Pesyan, Nader,Ojaghi Aghbash, Khadijeh

, (2021/10/05)

Green solventless preparation of dihydropyrano[3,2-b]chromenediones was developed by a three-component reaction (3-CR) of dimedone, different aldehydes, and kojic acid that catalyzed with nano-silica-MCM‐41‐kojic acid‐Ni as a reusable, efficient, and high

Acetic Acid-Mediated Synthesis of Kojic Acid Derivatives

Barbosa, L. C. A.,Kiran, Y. B.,Rambabu, G.,Vijayakumar, V.

, p. 1158 - 1166 (2021/09/08)

Abstract: A green acetic acid-mediated synthesis of kojic acid derivatives through amulticomponent reaction (MCR) has been developed. This new protocol is simpleand efficient; it involves a one-pot reaction of equimolar amounts of kojicacid, aromatic alde

Bcl3 catalyzed, solvent free protocol for the synthesis of dihydropyra-no[3,2-b] chromenediones

Dawle, Jairaj K.,Mathapati, Sushil R.,Momin, Kalimoddin I.,Suryawanshi, Vikas B.

, p. 400 - 406 (2021/09/07)

Solvent free synthesis of dihydropyrano[3,2-b]chromenediones was formulated via multi-component reactions of kojic acid, dimedone and several substituted aromatic aldehydes catalyzed with BCl3. Reactions progressed efficiently and the correspon

A meglumine catalyst–based synthesis, molecular docking, and antioxidant studies of dihydropyrano[3, 2-b]chromenedione derivatives

Sravya,Suresh,Zyryanov, Grigory V.,Balakrishna,Madhu Kumar Reddy,Suresh Reddy,Venkataramaiah,Rajendra,Bakthavatchala Reddy

, p. 355 - 369 (2019/11/28)

A simple method was employed for the synthesis of dihydropyrano[3, 2-b]chromenedione derivatives (4a-o) in high yields by condensation of 5, 5-dimethylcyclohexane-1, 3-dione(1), different aromatic aldehydes (2a-o), and 5-hydroxy-2-(hydroxymethyl)-4H-pyran

B(C6F5)3 catalyzed synthesis of dihydropyrano[3,2-b]chromenediones under solvent-free conditions

Sarnikar, Yuvaraj P.,Mane, Yogesh D.,Biradar, Dhanraj O.,Khade, Bhimrao C.

supporting information, p. 1143 - 1152 (2019/04/05)

A simple, efficient, solventless, and one step, B(C6F5)3 catalyzed, synthesis of dihydropyrano[3,2-b]chromenediones from dimedone, aldehyde and kojic acid is described. This protocol proceeds smoothly, accommodates aromati

Supramolecular catalysis by β-cyclodextrin for the synthesis of kojic acid derivatives in water

Kataev, Evgeny A.,Ramana Reddy, Mittapalli,Niranjan Reddy, Gangarpu,Reddy, Vemulapati Hanuman,Suresh Reddy, Cirandur,Subba Reddy, Basi V.

, p. 1693 - 1697 (2016/02/19)

An efficient and green method has been developed for the synthesis of kojic acid derivatives by employing 20 mol% β-cyclodextrin in aqueous media. The high functional group tolerance and shorter reaction times make this method suitable for the synthesis o

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