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40527-52-4

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40527-52-4 Usage

Description

(Z)-3-(4-methoxyphenyl)-2-methyl-prop-2-enoic acid, also known as ferulic acid, is a naturally occurring organic compound that belongs to the hydroxycinnamic acid family. It is predominantly found in the cell walls of certain plants and is prevalent in fruits, vegetables, nuts, and grains. Ferulic acid is recognized for its antioxidant properties, which contribute to its various applications in skincare, cosmetics, food preservation, and pharmaceuticals.

Uses

Used in Skincare and Cosmetics:
Ferulic acid is used as an additive in skincare and cosmetic products for its ability to protect against UV radiation and environmental damage. Its antioxidant properties help to maintain the health and appearance of the skin, making it a valuable component in anti-aging and skin-protective formulations.
Used in Food Preservation:
In the food industry, ferulic acid is utilized as a natural additive to extend the shelf life of products and maintain their freshness. Its antioxidant characteristics help to prevent the oxidation of fats and oils, which can lead to rancidity and spoilage.
Used in Pharmaceutical Research:
Ferulic acid is being researched for its potential use in the development of pharmaceuticals. Its anti-inflammatory and anti-cancer properties make it a promising candidate for the treatment of various chronic diseases and conditions.
Used in Drug Development:
The potential of ferulic acid in drug development is being explored due to its antioxidant and other beneficial properties. It may contribute to the creation of novel therapeutic agents for a range of health issues, including cancer and inflammation-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 40527-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40527-52:
(7*4)+(6*0)+(5*5)+(4*2)+(3*7)+(2*5)+(1*2)=94
94 % 10 = 4
So 40527-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-8(11(12)13)7-9-3-5-10(14-2)6-4-9/h3-7H,1-2H3,(H,12,13)/b8-7+

40527-52-4SDS

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-(4-methoxyphenyl)-2-methylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names (E)-2-methyl-3-(4-methoxyphenyl)propenoic acid

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:40527-52-4 SDS

40527-52-4Relevant articles and documents

Iwamoto

, p. 531 ()

Copper-Photocatalyzed Contra-Thermodynamic Isomerization of Polarized Alkenes

Bouillon, Jean-Philippe,Brégent, Thibaud,Poisson, Thomas

supporting information, p. 7688 - 7693 (2020/10/09)

The contra-thermodynamic isomerization of α- and β-substituted cinnamate derivatives catalyzed by the Cu(OAc)2/rac-BINAP complex under blue light irradiation is reported. The use of an oxazolidinone template, which favored the complexation of the copper catalyst to the substrate, allowed the E → Z isomerization of the catalytically formed chromophore under simple and robust reaction conditions in good to excellent ratios. The mechanism of this process based on the transient formation of a chromophore was also studied.

Enantioselective Cobalt-Catalyzed Sequential Nazarov Cyclization/Electrophilic Fluorination: Access to Chiral α-Fluorocyclopentenones

Zhang, Heyi,Cheng, Biao,Lu, Zhan

supporting information, p. 4028 - 4031 (2018/07/15)

A newly designed thiazoline iminopyridine ligand for enantioselective cobalt-catalyzed sequential Nazarov cyclization/electrophilic fluorination was developed. Various chiral α-fluorocyclopentenones were prepared with good yields and diastereo- and enantioselectivities. Further derivatizations could be easily carried out to provide chiral cyclopentenols with three contiguous stereocenters. Furthermore, a direct deesterification of fluorinated products could afford chiral α-single fluorine-substituted cyclopentenones.

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