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6-bromotetra-O-methylcatechin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88037-98-3

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88037-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88037-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88037-98:
(7*8)+(6*8)+(5*0)+(4*3)+(3*7)+(2*9)+(1*8)=163
163 % 10 = 3
So 88037-98-3 is a valid CAS Registry Number.

88037-98-3Relevant academic research and scientific papers

Proton magnetic resonance spectra of catechin and bromocatechin derivatives: C6- vs. C8-substitution

Kiehlmann, E.,Tracey, A. S.

, p. 1998 - 2005 (2007/10/02)

The 1Hmr spectra of 20 catechin derivatives substituted at C-6/C-8 by bromine and/or hydrogen and at oxygen by methyl, acetyl, and/or hydrogen have been analyzed in deuterated acetone, acetonitrile, and chloroform.Because of its dependence on the nature o

Synthesis of Condensed Tannins. Part 12. Direct Access to - and -all-2,3-cis-Procyanidin Derivatives from (-)-Epicatechin: Assessment of Bonding Positions in Oligomeric Analogues from Crataegus oxyacantha L.

Kolodziej, Herbert,Ferreira, Daneel,Roux, David G.

, p. 343 - 350 (2007/10/02)

Synthesis of methyl ester acetates of - and -all-2,3-cis-procyanidin biflavanoids is effected by oxidative functionalization of (-)-epicatechin tetramethyl ester with lead tetra-acetate, and condensation of the resultant 2,3-cis-flavan-3,4-diol

Tannins and Related Compounds. Part 13. Isolation and Structures of Trimeric, Tetrameric, and Pentameric Proanthicyanidins from Cinnamon

Nonaka, Gen-ichiro,Morimoto, Satoshi,Nishioka, Itsuo

, p. 2139 - 2145 (2007/10/02)

A proanthocyanidin trimer, two tetramers, and a pentamer have been isolated in their free phenolic forms from cinnamon, the bark of Cinnamomum zeylanicum (Lauraceae).Partial acid-catalysed degradation of these tannins with phenylmethanethiol, in conjunction with 1H- and 13C-n.m.r. analysis, has unequivocally established their structures as epicatechin-(4β->8, 2β->7)epicatechin-(4α->8)-epicatechin (5); epicatechin-(4β->8)epicatechin-(4β->8, 2β->7)-epicatechin-(4α->8)-epicatechin (6); epicatechin-(4β->6)-epicatechin-(4β->8, 2β->7)-epicatechin-(4α->8)-epicatechin (7); and epicatechin-(4β->8)-epicatechin-(4β->8)epicatechin-(4β->8, 2β->7)-epicatechin-(4α->8)-epicatechin (8).

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