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2,3-Bis[(E)-(4-hydroxy-3,5-dimethoxyphenyl)methylene]butanedioic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56136-37-9

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56136-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56136-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,3 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56136-37:
(7*5)+(6*6)+(5*1)+(4*3)+(3*6)+(2*3)+(1*7)=119
119 % 10 = 9
So 56136-37-9 is a valid CAS Registry Number.

56136-37-9SDS

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 diethyl (E,E)-2,3-bis(3,5-dimethoxy-4-hydroxybenzylidene)succinate

1.2 Other means of identification

Product number -
Other names bis-((E)-4-hydroxy-3,5-dimethoxy-benzylidene)-succinic acid diethyl 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:56136-37-9 SDS

56136-37-9Downstream Products

56136-37-9Relevant academic research and scientific papers

Sinapate dehydrodimers and sinapate-ferulate heterodimers in cereal dietary fiber

Bunzel, Mirko,Ralph, John,Kim, Hoon,Lu, Fachuang,Ralph, Sally A.,Marita, Jane M.,Hatfield, Ronald D.,Steinhart, Hans

, p. 1427 - 1434 (2007/10/03)

Two 8-8-coupled sinapic acid dehydrodimers and at least three sinapate-ferulate heterodimers have been identified as saponification products from different insoluble and soluble cereal grain dietary fibers. The two 8-8-disinapates were authenticated by comparison of their GC retention times and mass spectra with authentic dehydrodimers synthesized from methyl or ethyl sinapate using two different single-electron metal oxidant systems. The highest amounts (481 μg/g) were found in wild rice insoluble dietary fiber. Model reactions showed that it is unlikely that the dehydrodisinapates detected are artifacts formed from free sinapic acid during the saponification procedure. The dehydrodisinapates presumably derive from radical coupling of sinapate-polymer esters in the cell wall; the radical coupling origin is further confirmed by finding 8-8 and 8-5 (and possibly 8-0-4) sinapate-ferulate cross-products. Sinapates therefore appear to have an analogous role to ferulates in cross-linking polysaccharides in cereal grains and presumably grass cell walls in general.

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