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(2R,3S)-8-bromo-3,6-dihydroxy-5,7,3',4'-tetra-O-benzylflavan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848047-69-8

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848047-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848047-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,0,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 848047-69:
(8*8)+(7*4)+(6*8)+(5*0)+(4*4)+(3*7)+(2*6)+(1*9)=198
198 % 10 = 8
So 848047-69-8 is a valid CAS Registry Number.

848047-69-8Relevant academic research and scientific papers

Synthesis of modified proanthocyanidins: Easy and general introduction of a hydroxy group at C-6 of catechin; efficient synthesis of elephantorrhizol

Boyer, Francois-Didier,Es-Safi, Nour-Eddine,Beauhaire, Josiane,Le Guerneve, Christine,Ducrot, Paul-Henri

, p. 563 - 566 (2005)

A general procedure for the oxidation of catechin derivatives is described, leading to the introduction of a new hydroxy group at C-6. This procedure has been applied for the synthesis of elephantorrhizol, a natural flavan-3-ol exhibiting a fully substitu

Hydroxylation of ring A of flavan-3-ols: Influence of the ring A substitution pattern on the oxidative rearrangement of 6-hydroxyflavan-3-ols

Boyer, Francois-Didier,Beauhaire, Josiane,Martin, Marie Therese,Ducrot, Paul-Henri

, p. 3250 - 3260 (2008/09/16)

A general procedure for the oxidation of catechin derivatives is described, leading to the introduction of a new hydroxyl group at C-6. This procedure has been used for the synthesis of a number of 6-hydroxy flavan-3-ols, including elephantorrhizol, a natural flavan-3-ol exhibiting a fully substituted A ring. The substitution at C-8, albeit of poor influence on the course of this oxidation reaction, has been demonstrated to be preponderant for the further spontaneous oxidation and rearrangement of 6-hydroxy-flavan-3-ols into p-benzoquinones. The whole procedure allows the preparation of 6-alkyl substituted benzoquinones derived from catechin. Georg Thieme Verlag Stuttgart.

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