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7,2'-Dimethoxyisoflavanone is a naturally occurring chemical compound belonging to the class of flavanones, which are a type of flavonoid. It is characterized by the presence of two methoxy groups at the 7th position and the 2' position of the molecule. 7,2'-Dimethoxyisoflavanone is typically found in plants and has been identified in various species, including some medicinal plants. 7,2'-Dimethoxyisoflavanone is known for its potential antioxidant properties and is being studied for its possible biological activities, such as anti-inflammatory and anticancer effects. However, it is important to note that while these properties are of interest, further research is required to fully understand its therapeutic potential and safety profile.

5571-06-2

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5571-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5571-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5571-06:
(6*5)+(5*5)+(4*7)+(3*1)+(2*0)+(1*6)=92
92 % 10 = 2
So 5571-06-2 is a valid CAS Registry Number.

5571-06-2Downstream Products

5571-06-2Relevant academic research and scientific papers

Hydroxymethylation Studies of o-Hydroxyphenyl Benzyl Ketones with and without the use of Phase Transfer Catalyst: A Novel Synthesis of Isoflavanones

Jain, P. K.,Makrandi, J. K.,Grover, S. K.

, p. 51 - 58 (2007/10/02)

o-Hydroxyphenyl benzyl ketones, having a resorcinol unit in ring-A, on treatment with formalin in chloroform-aq. potassium carbonate biphase system give the corresponding α-hydroxymethyl derivatives.This reaction when carried out in the presence of a phas

A Convenient Phase Transfer Catalysed Synthesis of Isoflavanones

Singh, Harcharan,Jain, P. K.,Makrandi, J. K.,Grover, S. K.

, p. 547 - 548 (2007/10/02)

o-Hydroxyphenyl benzyl ketones (1, 4, 6, 8, 10, 12) on treatment with diiodomethane under phase transfer catalysed conditions in the presence of n-tetrabutylammonium iodide and sodium thiosulphate have been found to undergo smooth conversion into the corresponding isoflavanones (2, 5, 7, 9, 11, 13) in good yields (60-70percent).

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