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1-Imidazolidinecarboxylic acid, 3-methyl-2-oxo-4-(3-oxo-1-octenyl)-, phenylmethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90157-28-1

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90157-28-1 Usage

Molecular Structure

The compound is an ester derivative of imidazolidinecarboxylic acid, which means it contains a carbonyl group (C=O) bonded to an oxygen atom and an imidazolidine ring. The imidazolidine ring is a five-membered ring with two nitrogen atoms and one carbonyl group.

Double Bond in E Configuration

The compound has a double bond (C=C) in the E (trans) configuration, which means the two carbon atoms of the double bond are on opposite sides of the molecule. This configuration affects the compound's physical and chemical properties, such as its melting point, boiling point, and reactivity.

Antioxidant Properties

The compound may exhibit antioxidant properties, which could help protect cells from damage caused by free radicals. This makes it potentially useful in skincare and personal care products to prevent premature aging and other oxidative stress-related issues.

Antimicrobial Properties

The compound may have antimicrobial properties, which could help inhibit the growth of harmful microorganisms. This makes it suitable for use in cosmetic and pharmaceutical products to maintain a clean and healthy environment.

Anti-Inflammatory Properties

The compound may possess anti-inflammatory properties, which could help reduce inflammation and alleviate pain. This makes it potentially useful in the development of medications for treating various inflammatory conditions.

Bioactivity and Therapeutic Effects

The compound's chemical structure suggests potential bioactivity and therapeutic effects, which could lead to its development as a drug candidate for various medicinal purposes. Further research and testing are necessary to fully understand its properties and potential uses.

Applications in Pharmaceutical and Cosmetic Industries

Due to its potential properties, the compound may have applications in the pharmaceutical and cosmetic industries. It could be used in skincare products to protect against oxidative stress, in antimicrobial products to maintain a healthy environment, and as a potential drug candidate for various medicinal purposes.

Further Research and Testing

To fully understand the properties and potential uses of 1-Imidazolidinecarboxylic acid, 3-methyl-2-oxo-4-(3-oxo-1-octenyl)-, phenylmethyl ester, (E)-, further research and testing are necessary. This may include in vitro and in vivo studies, as well as clinical trials, to determine its safety, efficacy, and optimal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90157-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,5 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90157-28:
(7*9)+(6*0)+(5*1)+(4*5)+(3*7)+(2*2)+(1*8)=121
121 % 10 = 1
So 90157-28-1 is a valid CAS Registry Number.

90157-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-2-oxo-4-((E)-3-oxo-oct-1-enyl)-imidazolidine-1-carboxylic acid benzyl ester

1.2 Other means of identification

Product number -
Other names -

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:90157-28-1 SDS

90157-28-1Relevant academic research and scientific papers

Synthesis of Ethyl (+/-)-(E)-5-(4- and 5-(3-Hydroxy-1-octenyl)-1-methyl-2-imidazolin-2-yl)-5-thiapentanoates

Bartmann, W.,Beck, G.,Lau, H. H.,Wess, G.

, p. 733 - 736 (2007/10/02)

The racemic title compounds 1a,b and 2a,b were prepared from L-asparagine.

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