114612-78-1 Usage
General Description
The chemical compound 2,8:10,18-Dimethano-8H,14H,18H-pyrano[2,3-h']benzo[1,2-d:3,4-d']bis[1,3]benzodioxocin-5,7,13,15,19,21,22-heptol,2,10,16-tris(3,4-dihydroxyphenyl)-15,16-dihydro-, (2S,8R,10R,15R,16S,18R,21R,22R)-(9CI) is a complex compound with a long and detailed name. It contains multiple hydroxyl groups and phenyl moieties, indicating its potential role as a phenolic compound. The compound possesses a unique bicyclic structure with fused benzene and dioxocin rings, indicating potential biological activity and chemical reactivity. The stereochemistry, with specific R and S configurations at different positions, further contributes to the compound's overall structure and potential function. Further study and analysis of this compound are necessary to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 114612-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,1 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114612-78:
(8*1)+(7*1)+(6*4)+(5*6)+(4*1)+(3*2)+(2*7)+(1*8)=101
101 % 10 = 1
So 114612-78-1 is a valid CAS Registry Number.
114612-78-1Relevant articles and documents
Tannins and Related Compounds. LIX. Aesculitannins, Novel Proanthocyanidins with Doubly-Bonded Structures from Aesculus hippocastanum L.
Morimoto, Satoshi,Nonaka, Gen-ichiro,Nishioka, Itsuo
, p. 4717 - 4729 (2007/10/02)
A chemical examination of the seed shells of Aesculus hyppocastanum L.has led to the isolation of proanthocyanidins A-6 (10) and A-7 (11), and aesculitannins A (12), B (13), C (14), D (15), E (16), F (17) and G (18).On the basis of chemical and spectroscopic evidence, proanthocyanidins A-6 (10) and A-7 (11) have been determined to be A-type dimers each possessing a C-4, C-6 interflavanoid linkage, while aesculitannins A (12), B (13), C (14), D (15), E (16), F (17) and G (18) have been characterized as oligomeric proanthocyanidins possessing A-type unit(s) in each molecule.In addition, the presence of (-)-epicatechin (1), proanthocyanidins B-5 (3), A-2 (4), A-4 (5) and C-1 (6), epicatechin-(4β->6)-epicatechin-(4β->6)-epicatechin (7), and cinnamtannins B1 (8) and B2 (9) was also demonstrated Keywords---Aesculus hippocastanum; Hippocastanaceae; aesculitannin; doubly-bonded proanthocyanidin; procyanidin; condensed tannin; flavan-3-ol; thiolytic degradation; epimerization; hydrogen peroxide oxidation
