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1,5-Cyclohexadiene-1-carboxylic acid, 3,4-dioxo-5-(phenylmethoxy)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169229-46-3

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169229-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169229-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,2 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169229-46:
(8*1)+(7*6)+(6*9)+(5*2)+(4*2)+(3*9)+(2*4)+(1*6)=163
163 % 10 = 3
So 169229-46-3 is a valid CAS Registry Number.

169229-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 3-(benzyloxy)-1,2-dioxocyclohexa-3,5-diene-5-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Benzyloxy-3,4-dioxo-cyclohexa-1,5-dienecarboxylic acid benzyl ester

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:169229-46-3 SDS

169229-46-3Relevant academic research and scientific papers

Galloyl-derived orthoquinones as reactive partners in nucleophilic additions and Diels-Alder dimerizations: A novel route to the dehydrodigalloyl linker unit of agrimoniin-type ellagitannins

Feldman, Ken S.,Quideau, Stephane,Appel, Heidi M.

, p. 6656 - 6665 (2007/10/03)

Orthochloranil-mediated oxidation of galloyl monoethers furnishes the derived orthoquinones in excellent yield. These reactive electrophiles participate in a variety of nucleophilic addition reactions with heteroatomic and carbanionic partners. In addition, Lewis acid-mediated dimerization of the orthoquinones provides an efficient route to dehydrodigalloyl-type diaryl ether units characteristic of several ellagitannin natural products. The implications for ellagitannin biosynthesis and gallotannin-protein covalent attachment are discussed.

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