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59576-98-6

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59576-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59576-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,7 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59576-98:
(7*5)+(6*9)+(5*5)+(4*7)+(3*6)+(2*9)+(1*8)=186
186 % 10 = 6
So 59576-98-6 is a valid CAS Registry Number.

59576-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name p-coumaramide

1.2 Other means of identification

Product number -
Other names trans-4-hydroxycinnamide

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:59576-98-6 SDS

59576-98-6Downstream Products

59576-98-6Relevant articles and documents

METHODS OF REDUCING VIRULENCE IN BACTERIA

-

Page/Page column 76; 88, (2011/09/19)

A method of reducing virulence in a bacterium comprising at least one of a GacS/GacA-type system, a HrpX/HrpY-type system, a T3SS-type system, and a Rsm-type system, the method comprising contacting the bacterium with an effective amount of a compound described herein.

Isolation and Activity of N-p-Coumaroyltyramine, an α-Glucosidase Inhibitor in Welsh Onion (Allium fistulosum)

Nishioka, Tetsuo,Watanabe, Jun,Kawabata, Jun,Niki, Ryoya

, p. 1138 - 1141 (2007/10/03)

A phenolic amide, N-p-coumaroyltyramine (1), was isolated as an α-glucosidase inhibitor from methanol extracts of Welsh onion (Allium fistulosum). The inhibitory activity of 1 against a yeast enzyme was as high as Ki 8.4 × 10-7 M. From a structure-activity relationship study of 1 and its related compounds, the occurrence of α-glucosidase inhibitory activity required a p-coumaramide structure, with an amide hydrogen and alkyl or aralkyl substituent on the amide part.

COMPARATIVE REACTIVITY OF NITRILES OF PARA-SUBSTITUTED CINNAMIC ACIDS IN THE ALKYLATION OF BENZENE IN THE PRESENCE OF ALUMINUM CHLORIDE

Grebenyuk, A. D.,Grinshpun, V. D.,L'vov, V. M.

, p. 732 - 736 (2007/10/02)

The relative rate constants for the reactions of the nitriles of p-methoxy, p-methyl, and p-chlorocinnamic acids with benzene in the presence of aluminum chloride were determined by the method of competing reactions in relation to cinnamonitrile.The negative sign of ρ indicates that the electrophilic stage of complex formation between the unsaturated nitrile and aluminum chloride has a deciding role in the alkylation process.

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