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Cis-Isoflavan-4-ol is a naturally occurring organic compound belonging to the isoflavonoid class, which is derived from flavonoids. It is characterized by its specific molecular structure, featuring a cis-configuration around the double bond between carbons 2 and 3. cis-Isoflavan-4-ol is known for its antioxidant properties and is found in certain plants, where it plays a role in plant defense mechanisms against pathogens and environmental stress. Cis-Isoflavan-4-ol has also been studied for its potential health benefits, including its impact on hormonal balance and its antioxidant activity, which may contribute to its potential use in pharmaceutical and nutraceutical applications.

6212-70-0

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6212-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6212-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6212-70:
(6*6)+(5*2)+(4*1)+(3*2)+(2*7)+(1*0)=70
70 % 10 = 0
So 6212-70-0 is a valid CAS Registry Number.

6212-70-0Downstream Products

6212-70-0Relevant academic research and scientific papers

Formation of hydridocobalt(iii) phthalocyanine by reaction of cobalt(ii) phthalocyanines with sodium borohydride and its reactions with antioxidant isoflavones

Poonam,Kumari, Pratibha,Nagpal, Ritika,Chauhan, Shive M. S.

experimental part, p. 2639 - 2646 (2012/01/04)

The reduction of substituted isoflavones with sodium borohydride catalyzed by cobalt(ii) phthalocyanines has been achieved efficiently to yield cis- and trans-isoflavan-4-ols under mild conditions via the formation of a hydridocobalt(iii) phthalocyanine i

Experimental and DFT 1H NMR study of conformational equilibria in trans-4′,7-dihydroxyisoflavan-4-ol and trans-isoflavan-4-ol

Pihlaja, Kalevi,Taehtinen, Petri,Klika, Karel D.,Jokela, Tuija,Salakka, Auli,Waehaelae, Kristiina

, p. 6864 - 6869 (2007/10/03)

The solution-state conformational equilibria of trans-4′ ,7-dihydroxyisoflavan-4-ol (1) and transisoflavan-4-ol (2) were assessed based on the temperature dependence of their vicinal coupling constants J H-2α,H-3 and JH-3,H-4 in comp

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