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19272-90-3

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19272-90-3 Usage

General Description

4-HYDROXY-3-METHOXYCINNAMIDE is a chemical compound with the molecular formula C10H11NO3. It is a derivative of cinnamamide and has a hydroxyl group and a methoxy group attached to the cinnamamide backbone. 4-HYDROXY-3-METHOXYCINNAMIDE has potential biological activities, including anti-inflammatory and antioxidant properties. It is also used in the pharmaceutical industry as a building block for the synthesis of other compounds. Additionally, it has been studied for its potential use in the treatment of various diseases and disorders, including cancer and neurodegenerative diseases. Overall, 4-HYDROXY-3-METHOXYCINNAMIDE is a versatile compound with potential applications in medicine and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 19272-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19272-90:
(7*1)+(6*9)+(5*2)+(4*7)+(3*2)+(2*9)+(1*0)=123
123 % 10 = 3
So 19272-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-14-9-6-7(2-4-8(9)12)3-5-10(11)13/h2-6,12H,1H3,(H2,11,13)/b5-3+

19272-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names 3-(4-Hydroxy-3-methoxyphenyl)-2-propenamide

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:19272-90-3 SDS

19272-90-3Downstream Products

19272-90-3Relevant articles and documents

A Thorough Study on the Photoisomerization of Ferulic Acid Derivatives

Moni, Lisa,Banfi, Luca,Basso, Andrea,Mori, Alessia,Risso, Federica,Riva, Renata,Lambruschini, Chiara

, p. 1737 - 1749 (2021/03/23)

A thorough study on the (E) to (Z) photoisomerization of ferulic acid derivatives (esters, amides of all types, and ketones) was carried out. At the photostationary state, only aliphatic or benzylic tertiary amides reach a nearly complete conversion of (E) isomers into the (Z) ones, whereas for esters, primary and secondary amides or aromatic tertiary amides mixtures of (Z)/(E) ranging from 7 : 93 to 72 : 28 are observed. Ketones show rather limited photoisomerization. However, (Z) ketones may be obtained by the reaction of organometal compounds with an isomerized (Z) Weinreb amide.

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