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Trans-7-methoxyisoflavan-4-ol is a naturally occurring isoflavonoid compound, characterized by its unique chemical structure that includes a methoxy group at the 7th position and a hydroxyl group at the 4th position. Isoflavonoids are a subgroup of flavonoids, which are widely found in plants and are known for their diverse biological activities. Trans-7-methoxyisoflavan-4-ol, in particular, is known for its potential antioxidant properties and is typically extracted from plant sources such as the heartwood of certain trees. trans-7-methoxyisoflavan-4-ol has been the subject of scientific interest due to its potential health benefits, including its role in reducing oxidative stress and its possible impact on hormone regulation. However, further research is needed to fully understand its mechanisms of action and potential applications in medicine or nutrition.

4281-30-5

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4281-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4281-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4281-30:
(6*4)+(5*2)+(4*8)+(3*1)+(2*3)+(1*0)=75
75 % 10 = 5
So 4281-30-5 is a valid CAS Registry Number.

4281-30-5Downstream Products

4281-30-5Relevant academic research and scientific papers

Enantioselective Synthesis of Isoflavanones by Catalytic Dynamic Kinetic Resolution

Qin, Tao,Metz, Peter

supporting information, p. 2981 - 2984 (2017/06/07)

A ruthenium-catalyzed asymmetric transfer hydrogenation of racemic isoflavanones with dynamic kinetic resolution yields virtually enantiopure isoflavanols as single diastereomers. Subsequent oxidation gives rise to isoflavanones in high enantiomeric purit

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

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