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[4,8':4',8'':4'',8'''-Quater-2H-1-benzopyran]-3,- 3',3'',3''',5,5',5'',5''',7,7',7'',7'''-dodecol,2,2',2'',- 2'''-tetrakis(3,4-dihydroxyphenyl)-3,3',3'',3''',4,- 4',4'',4'''-octahydro-,(2R,2'R,2''R,2'''R,3R,3'R,- 3''R,3'''S,4R,4'R,4''S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79763-29-4

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79763-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79763-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79763-29:
(7*7)+(6*9)+(5*7)+(4*6)+(3*3)+(2*2)+(1*9)=184
184 % 10 = 4
So 79763-29-4 is a valid CAS Registry Number.

79763-29-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name epicatechin-(4β-8)-epicatechin-(4β-8)-epicatechin-(4β-8)-catechin

1.2 Other means of identification

Product number -
Other names arecatannin A-2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79763-29-4 SDS

79763-29-4Downstream Products

79763-29-4Relevant academic research and scientific papers

Versatile synthesis of epicatechin series procyanidin oligomers, and their antioxidant and DNA polymerase inhibitory activity

Saito, Akiko,Mizushina, Yoshiyuki,Tanaka, Akira,Nakajima, Noriyuki

experimental part, p. 7422 - 7428 (2009/12/24)

Proanthocyanidins, known as condensed tannins or oligomeric flavonoids, exist in many edible plants and show various interesting biological activities. We have developed a simple and versatile method of synthesizing procyanidin oligomers consisting of (-)

Synthesis of Condensed Tannins. Part 13. The First 2,3-trans-3,4-cis-Procyanidins: Sequence of Units in a 'Trimer' of Mixed Stereochemistry

Delcour, Jan A.,Serneels, Edward J.,Ferreira, Daneel,Roux, David G.

, p. 669 - 676 (2007/10/02)

The condensation of (+)-leucocyanidin with (-)-epicatechin initiates a succession of substitutions leading mainly to the introduction of -2,3-trans-3,4-procyanidin units, but also to the incorporation of 'terminal' moieties which possess the hitherto unique 3,4-cis-procyanidin configuration.The bonding patterns in the products, and also the sequence of units in one of the 'trimers' of mixed stereochemistry, are resolved by (1)H n.m.r. spectroscopy through selective use of solvents at elevated temperatures.

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