121844-27-7 Usage
Uses
Used in Pharmaceutical Industry:
Benzoic acid,3,4,5-trihydroxy-,(1R,2R)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure and biochemical activity make it a promising candidate for the development of new drugs and treatments.
Used in Drug Discovery and Development:
In the field of drug discovery and development, Benzoic acid,3,4,5-trihydroxy-,(1R,2R)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) serves as a valuable starting point for the synthesis of novel compounds with potential medicinal properties. Its structural diversity and functional groups provide a foundation for further chemical modifications and optimization to enhance its therapeutic potential.
Used in Biochemical Research:
Benzoic acid,3,4,5-trihydroxy-,(1R,2R)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) is utilized in biochemical research to study its interactions with biological systems and understand its potential mechanisms of action. This knowledge can contribute to the development of new therapeutic strategies and the identification of novel drug targets.
Check Digit Verification of cas no
The CAS Registry Mumber 121844-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,4 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121844-27:
(8*1)+(7*2)+(6*1)+(5*8)+(4*4)+(3*4)+(2*2)+(1*7)=107
107 % 10 = 7
So 121844-27-7 is a valid CAS Registry Number.
121844-27-7Relevant academic research and scientific papers
Tannins and Related Compounds. LXXVII. Novel Chalcan-flavan Dimers, Assamicains A, B and C, and a New Flavan-3-ol and Proanthocyanidins from the Fresh Leaves of Camellia sinensis L. var. assamica KITAMURA
Hashimoto, Fumio,Nonaka, Gen-ichiro,Nishioka, Itsuo
, p. 77 - 85 (2007/10/02)
Three novel chalcan-flavan dimers, assamicains A (1), B (2) and C (3), and a new flavan-3-ol (14) and proanthocyanidins (19,20) have been isolated, together with the known flavan-3-ols (4-13), proanthocyanidins (15-18,21), theasinensins (22-24) and hydrolyzable tannins (25,26), from the fresh leaves of Camellia sinensis var. assamica (Camelliaceae), and their structures have been established on the basis of spectroscopic evidence in conjunction with thiolytic degradation and enzymatic hydrolysis. - Keywords: Camellia sinensis var. assamica; Camelliaceae; polyphenol; assamicain; chalcan-flavan dimer; proanthocyanidin; theasinensin; flavan-3-ol; hydrolyzable tannin; black tea
