64121-98-8 Usage
Description
Di-O-Methylcrenatin is a monosaccharide derivative that consists of 4-(hydroxymethyl)-2,6-dimethoxyphenol attached to a beta-D-glucopyranosyl residue at position 1 via a glycosidic linkage. It is isolated from Acacia mearnsii and exhibits cytotoxic activity.
Uses
Used in Pharmaceutical Industry:
Di-O-Methylcrenatin is used as a pharmaceutical compound for its cytotoxic properties. The expression is: Di-O-Methylcrenatin is used as a cytotoxic agent for its ability to exhibit cytotoxic activity, making it a potential candidate for the development of therapeutic treatments.
Used in Cancer Research:
In the field of cancer research, Di-O-Methylcrenatin is used as a research tool to study the mechanisms of cytotoxicity and its potential application in the development of anti-cancer drugs. The expression is: Di-O-Methylcrenatin is used as a research tool for understanding cytotoxic mechanisms and its potential role in cancer treatment.
Used in Drug Development:
Di-O-Methylcrenatin is used as a starting material or intermediate in the synthesis of other bioactive compounds with potential therapeutic applications. The expression is: Di-O-Methylcrenatin is used as a starting material for the development of new bioactive compounds with potential pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 64121-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,2 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64121-98:
(7*6)+(6*4)+(5*1)+(4*2)+(3*1)+(2*9)+(1*8)=108
108 % 10 = 8
So 64121-98-8 is a valid CAS Registry Number.
64121-98-8Relevant articles and documents
Tannins and Related Compounds. LXIV. Six New Phenol Glucoside Gallates from Castanopsis cuspidata var. sieboldii NAKAI. (2)
Ageta, Masayuki,Ishimaru, Kanji,Nonaka, Gen-Ichiro,Nishioka, Itsuo
, p. 870 - 876 (2007/10/02)
Six new phenol glucoside gallates (3-5, 7, 9 and 10) have been isolated from Castanopsis cuspidata var. sieboldii NAKAI (Fagaceae), together with the known compounds, dehydrodigallic acid (1), cretanin (2), chesnatin (11) and chestanin (8).On the basis of spectroscopic evidence and the result of tannase hydrolysis, the structures of compounds 3-5 have been established to be the mono- (3) and digallates (4 and 5) of crenatin (6).Similarly, compounds 7, 9 and 10 have been characterized as the monogallate (7) of 3,4-dihydroxyphenethyl alcohol 4-O-β-D-glucopyranoside and the monogallates (9 and 10) of 8.In addition, the structure of chesnatin (11), in which the orientation of the dehydrodigalloyl group had been unknown, was determined by detailed carbon-13 nuclear magnetic resonance examination.Keywords - Castanopsis cuspidata var. sieboldii; Fagaceae; phenol glucoside gallate; 3,4,5-trihydroxybenzyl alcohol; 3,4-dihydroxyphenethyl alcohol; dehydrodigallic acid; chesnatin
