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3-(2-Ethoxyphenyl)propionic acid is an organic compound belonging to the phenylpropanoid and polyketide class. It features a phenylpropanoid moiety with a three-carbon side chain and a 2-ethoxyphenyl substituent at the 3-position of a propionic acid structure. This chemical is primarily found in the biofluids, tissues, and feces of mammals and is associated with the metabolic breakdown of certain drugs or compounds within the body.

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  • 220285-28-9 Structure
  • Basic information

    1. Product Name: 3-(2-ETHOXYPHENYL)PROPIONIC ACID
    2. Synonyms: 3-(2-ETHOXYPHENYL)PROPANOIC ACID;3-(2-ETHOXYPHENYL)PROPIONIC ACID;2-Ethoxybenzenepropanoic acid
    3. CAS NO:220285-28-9
    4. Molecular Formula: C11H14O3
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: Aromatic Propionic Acids
    8. Mol File: 220285-28-9.mol
  • Chemical Properties

    1. Melting Point: 77-82℃
    2. Boiling Point: 319.1 °C at 760 mmHg
    3. Flash Point: 121.9 °C
    4. Appearance: /
    5. Density: 1.116 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 4.73±0.10(Predicted)
    10. CAS DataBase Reference: 3-(2-ETHOXYPHENYL)PROPIONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2-ETHOXYPHENYL)PROPIONIC ACID(220285-28-9)
    12. EPA Substance Registry System: 3-(2-ETHOXYPHENYL)PROPIONIC ACID(220285-28-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 220285-28-9(Hazardous Substances Data)

220285-28-9 Usage

Uses

Since the provided materials do not specify any particular applications for 3-(2-Ethoxyphenyl)propionic acid, it is not possible to list its uses based on the given information. However, its presence in the biofluids, tissues, and feces of mammals suggests that it may have potential roles in biological processes or as a metabolic byproduct. Further research would be required to explore its potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 220285-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,8 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 220285-28:
(8*2)+(7*2)+(6*0)+(5*2)+(4*8)+(3*5)+(2*2)+(1*8)=99
99 % 10 = 9
So 220285-28-9 is a valid CAS Registry Number.

220285-28-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H33569)  3-(2-Ethoxyphenyl)propionic acid, 96%   

  • 220285-28-9

  • 1g

  • 336.0CNY

  • Detail
  • Alfa Aesar

  • (H33569)  3-(2-Ethoxyphenyl)propionic acid, 96%   

  • 220285-28-9

  • 5g

  • 1117.0CNY

  • Detail
  • Alfa Aesar

  • (H33569)  3-(2-Ethoxyphenyl)propionic acid, 96%   

  • 220285-28-9

  • 25g

  • 3200.0CNY

  • Detail

220285-28-9SDS

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 3-(2-ethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(2-Ethoxyphenyl)propanoic 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:220285-28-9 SDS

220285-28-9Downstream Products

220285-28-9Relevant articles and documents

Small molecule inhibitors of anthrax lethal factor toxin

Williams, John D.,Khan, Atiyya R.,Cardinale, Steven C.,Butler, Michelle M.,Bowlin, Terry L.,Peet, Norton P.

, p. 419 - 434 (2014/01/17)

This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds.

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