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2-(3-hydroxy-4-methoxyphenyl)chroman-4-one is a complex organic compound with the molecular formula C16H14O4. It is a derivative of chroman-4-one, which is a heterocyclic compound consisting of a benzene ring fused to a pyran ring. The compound features a hydroxy group at the 3-position and a methoxy group at the 4-position on the phenyl ring, which is attached to the chroman-4-one structure. This specific arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's structure and properties make it an interesting target for further research and development.

1621-70-1

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1621-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1621-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1621-70:
(6*1)+(5*6)+(4*2)+(3*1)+(2*7)+(1*0)=61
61 % 10 = 1
So 1621-70-1 is a valid CAS Registry Number.

1621-70-1Relevant academic research and scientific papers

Synthesis and evaluation of novel carbamate-substituted flavanone derivatives as potent acetylcholinesterase inhibitors and anti-amnestic agents

Anand, Preet,Singh, Baldev

, p. 1648 - 1659 (2013/07/26)

This study was designed to synthesize and evaluate flavanone derivatives with phenylcarbamate moiety as potent acetylcholinesterase (AChE) inhibitors and anti-amnestic agents for management of AD. The synthesis of carbamate-substituted flavanone derivativ

Aromatic ring hydroxylation of flavanones by dimethyldioxirane

Bernini, Roberta,Mincione, Enrico,Sanetti, Anna,Mezzetti, Maurizio,Bovicelli, Paolo

, p. 1087 - 1090 (2007/10/03)

The selective and efficient oxidation of flavanones with dimethyldioxirane (DMD) is reported. Aromatic rings carrying methoxy groups were selectively hydroxylated in neutral and acidic media. In the latter case inversion of chemoselectivity with respect to the benzylethereal position was observed. This behaviour was exploited to obtain polyhydroxylated flavanones, which are compounds with potential antioxidant and biological properties. (C) 2000 Elsevier Science Ltd.

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