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56279-88-0

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56279-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56279-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,7 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56279-88:
(7*5)+(6*6)+(5*2)+(4*7)+(3*9)+(2*8)+(1*8)=160
160 % 10 = 0
So 56279-88-0 is a valid CAS Registry Number.

56279-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-succinimidyl sinapate

1.2 Other means of identification

Product number -
Other names (E)-3-(4-Hydroxy-3,5-dimethoxy-phenyl)-acrylic acid 2,5-dioxo-pyrrolidin-1-yl 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:56279-88-0 SDS

56279-88-0Downstream Products

56279-88-0Relevant articles and documents

Vir-gene-inducing activities of hydroxycinnamic acid amides in Agrobacterium tumefaciens

Berthelot, Karine,Buret, David,Guerin, Brigitte,Delay, Didier,Negrel, Jonathan,Delmotte, Francis M.

, p. 1537 - 1548 (1998)

Expression of Agrobacterium tumefaciens virulence genes and transformation of dicots by this organism are dependent upon host plant phenolic compounds. Several alkylsyringamides have recently been shown to be powerful inducers of these vir-genes. These synthetic amides, and especially ethylsyringamide, are much stronger inducers than syringic acid. In this work, four alkylamides derived from ferulic or sinapic acids were synthesized by a dicyclohexylcarbodiimide method and tested for their potential to induce vir-gene expression on A. tumefaciens strains harbouring virB::lacZ or virE::lacZ fusion plasmids. Their effectiveness was compared to that of ethylsyringamide and tyraminylferulamide, a naturally occurring amide in plants. Whatever the amine moiety of the amide (ethylamine, propylamine, tyramine or β-alanine ethyl ester) conjugation of the acid functional group clearly diminished the toxicity to the bacteria of the respective acid at high concentration and thereby increased the vir-inducing potential. However, none of the inducers tested exhibited higher activity than acetosyringone, the reference compound for vir-gene induction, with the exception of ethylsyringamide at concentrations above 1 mM. When tested on Agrobacterium tumefaciens strain A348(pSM243cd), ethylferulamide and ethylsinapamide were more efficient than the corresponding phenolic acids but only above 100 μM.

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