Welcome to LookChem.com Sign In|Join Free
  • or
2,4-Pentadienoic acid, 5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)is a complex chemical compound, also known as ethyl sorbate. It is an ethyl ester derivative of 2,4-pentadienoic acid, characterized by a chain of carbon atoms with multiple double bonds and methoxy groups. 2,4-Pentadienoic acid,
5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)possesses unique properties due to its chemical structure, making it suitable for various applications. However, its complex nature and potential reactivity require careful handling and use.

101619-49-2

Post Buying Request

101619-49-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

101619-49-2 Usage

Uses

Used in Food Industry:
2,4-Pentadienoic acid, 5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)is used as a flavoring agent and preservative in the food industry. Its pleasant aroma and antimicrobial properties make it an effective ingredient in enhancing the taste and extending the shelf life of various food products.
Used in Flavoring Agents:
In the flavoring industry, 2,4-Pentadienoic acid, 5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)is used to impart a desirable aroma to food products. Its unique scent profile contributes to the overall sensory experience of the products, making them more appealing to consumers.
Used in Antimicrobial Agents:
2,4-Pentadienoic acid, 5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)is also used as an antimicrobial agent in the food industry. Its ability to inhibit the growth of microorganisms helps maintain the freshness and safety of food products, reducing the risk of spoilage and contamination.
Used in Chemical Synthesis:
Due to its complex structure and unique properties, 2,4-Pentadienoic acid, 5-[3-methoxy-4-[(2-methoxyethoxy)methoxy]phenyl]-, ethyl ester, (E,E)can be used as a starting material or intermediate in the synthesis of other chemical compounds. Its reactivity and functional groups make it a valuable component in the development of new materials and products in various industries, such as pharmaceuticals, cosmetics, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 101619-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,1 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101619-49:
(8*1)+(7*0)+(6*1)+(5*6)+(4*1)+(3*9)+(2*4)+(1*9)=92
92 % 10 = 2
So 101619-49-2 is a valid CAS Registry Number.

101619-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-5-[3-Methoxy-4-(2-methoxy-ethoxymethoxy)-phenyl]-penta-2,4-dienoic acid ethyl 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:101619-49-2 SDS

101619-49-2Upstream product

101619-49-2Relevant academic research and scientific papers

(2E,4E)-N-(4-(1H-indol-3-yl)piperidin-1-yl)alkyl-5-(substituted phenyl)-2,4-pentadienamides as antiallergic agents with antihistaminic and anti slow-reacting substance (SRS) activities

Shigenaga,Manabe,Matsuda,Fujii,Matsuo

, p. 3 - 10 (2007/10/02)

As an extension of our study aiming to discover a novel compound with dual activities against histamine and slow-reacting substance (SRS), we synthesized two types of indolylpiperidine derivatives, 3 and 4-20. Testing for in vivo antianaphylactic activity and for in vitro anti-SRS activity revealed that (2E,4E)-5-(3,5-dimethoxy-4-hydroxyphenyl)-N-(2-(4-(1H-indol-3-yl)piper idin-1-yl)ethyl)-2,4-pentadienamide (11) exhibited potent dual activities with ED50 = 0.89 mg/kg and IC50 = 1.43 μM, respectively. However, the plasma concentration of unchanged 11 was very low when administered orally in guinea pigs. This result can be explained by fast formation of a glucuronic acid conjugate.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 101619-49-2