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2-amino-6-(hydroxymethyl)-8-oxo-4-(3-pyridinyl)-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

625376-09-2

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625376-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 625376-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,3,7 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 625376-09:
(8*6)+(7*2)+(6*5)+(5*3)+(4*7)+(3*6)+(2*0)+(1*9)=162
162 % 10 = 2
So 625376-09-2 is a valid CAS Registry Number.

625376-09-2Downstream Products

625376-09-2Relevant academic research and scientific papers

Green synthesis of pyrano [3,2-b]pyran derivatives using nano Si–Mg–fluorapatite catalyst and the evaluation of their antibacterial and antioxidant properties

Ostadsharif Memar, Fardad,Khazdooz, Leila,Zarei, Amin,Abbaspourrad, Alireza

, p. 1792 - 1803 (2020/07/15)

In this study, we synthesize 2-amino-4-alkyl/aryl-6-(hydroxymethyl)-8-oxopyrano[3,2-b] pyran-3-carbonitriles derivatives using a multicomponent reaction featuring aromatic or aliphatic aldehydes, kojic acid, and malononitrile catalyzed by nano fluoroapati

Ultrasound promoted one-pot synthesis of 2-amino-4,8-dihydropyrano[3,2-b] pyran-3-carbonitrile scaffolds in aqueous media: A complementary 'green chemistry' tool to organic synthesis

Banitaba, Sayed Hossein,Safari, Javad,Khalili, Shiva Dehghan

supporting information, p. 401 - 407 (2013/01/15)

A green and simple approach to assembling of 2-amino-4,8-dihydropyrano[3,2- b]pyran-3-carbonitrile scaffolds via three-component reaction of kojic acid, malononitrile, and aromatic aldehydes in aqueous media under ultrasound irradiation is described. The combinatorial synthesis was achieved for this methodology with applying ultrasound irradiation while making use of water as green solvent. In comparison to conventional methods, experimental simplicity, good functional group tolerance, excellent yields, short routine, and selectivity without the need for a transition metal or base catalyst are prominent features of this green procedure.

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