610778-85-3 Usage
Uses
Used in Pharmaceutical Industry:
Isobonducellin is used as a pharmaceutical agent for its anti-inflammatory and anti-cancer properties. Its natural occurrence and potential to alleviate inflammation and combat cancer make it a promising candidate for the development of new treatments and therapies.
Used in Natural Remedies:
In the field of natural medicine, Isobonducellin is utilized for its potential health benefits. Its presence in Bonduc tree species suggests that it could be incorporated into herbal remedies and supplements aimed at reducing inflammation and supporting cancer treatment.
Used in Research and Development:
Isobonducellin is employed as a subject of research in the scientific community. Its unique structure and biological activity are being investigated to understand its full potential and to develop new pharmaceutical compounds and applications based on its properties.
Check Digit Verification of cas no
The CAS Registry Mumber 610778-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,7,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 610778-85:
(8*6)+(7*1)+(6*0)+(5*7)+(4*7)+(3*8)+(2*8)+(1*5)=163
163 % 10 = 3
So 610778-85-3 is a valid CAS Registry Number.
610778-85-3Relevant academic research and scientific papers
Synthesis, stereochemical assignments, and biological activities of homoisoflavonoids
Siddaiah, Vidavalur,Rao, Chunduri Venkata,Venkateswarlu, Somepalli,Krishnaraju, Alluri V.,Subbaraju, Gottumukkala V.
, p. 2545 - 2551 (2007/10/03)
A series of four naturally occurring homoisoflavonoids and eight analogs have been synthesized starting from an appropriately substituted phenol through chroman-4-one, in four steps. The products were assigned as E-isomers based on NMR spectroscopic data.
Chemistry of Homoisoflavonoids: Synthesis of Polyhydroxy 3-Benzylchromones and 3-Benzylchroman-4-ones without Protection and Deprotection of Hydroxyl Groups and a Convenient Preparation of Benzylidenechroman-4-ones
Sathyanarayana, S.,Krishnamurty, H. G.
, p. 899 - 901 (2007/10/02)
Catalytic transfer hydrogenation of hydroxyflavanones gives hydroxydihydrochalcones.These dihydrochalcones are converted into hydroxyhomoisoflavones and homoisoflavanones without protection and deprotection of hydroxyl groups.The condensation between chromanones and aryl aldehydes in the presence of dry p-toluenesulfonic acid in benzene or toluene gives benzylidenechromanones in good yields.The method is far superior to all other existing procedures.
