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CAS

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14737-88-3

2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-, (Z)-, also known as (Z)-3-(3,4-dimethoxyphenyl)acrylic acid, is an organic compound characterized by its molecular formula C11H12O4. 2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-, (Z)- features a 3,4-dimethoxyphenyl group attached to the 3-position of the acrylic acid backbone, which is in the Z-configuration, indicating the geometric arrangement of the double bond. It is a colorless to pale yellow crystalline solid with a molecular weight of 208.21 g/mol. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that handling and storage of 2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-, (Z)- should be done with care, adhering to safety protocols, as it may have potential health and environmental impacts.

14737-88-3

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14737-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14737-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,3 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14737-88:
(7*1)+(6*4)+(5*7)+(4*3)+(3*7)+(2*8)+(1*8)=123
123 % 10 = 3
So 14737-88-3 is a valid CAS Registry Number.

14737-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,4-dimethoxyphenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names cis-3.4-Dimethoxy-zimtsaeure

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:14737-88-3 SDS

14737-88-3Relevant articles and documents

Understanding the role played by protic ionic liquids (PILs) and the substituent effect for enhancing the generation of: Z-cinnamic acid derivatives

Rodríguez, Roció B.,Rodríguez, Roció B.,Zapata, Ramiro L.,Salum, Mariá L.,Salum, Mariá L.,Erra-Balsells, Rosa,Erra-Balsells, Rosa

, p. 819 - 830 (2020/07/03)

Photoisomerization of a series of substituted E-cinnamic acids in MeCN in their acid forms and as their corresponding protic ionic liquids (PILs) with light of 300 nm is studied. The nature, strength, number, and position effects of substituents on the photochemical behavior of E-cinnamic derivatives are investigated. The photosensitization of the reaction in the presence of Michler's ketone is also studied at 366 nm and it demonstrates that the triplet-excited state is involved in the reaction. As the presence of n-butylamine needed to form the PILs significantly increases the photoproduct yields in all cases, the role of the PILs is also discussed. Thus, understanding of these fundamental aspects has allowed us to establish an excellent and practical synthetic protocol for successfully synthesizing Z-cinnamic acids. This journal is

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