Welcome to LookChem.com Sign In|Join Free
  • or
(2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE, also known as D-DOPAA, is an amino acid derivative with the molecular formula C9H11N3O2. It is a chiral molecule, meaning it has a non-superimposable mirror image. (2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is commonly used in research and pharmaceutical applications due to its potential biological activity. Some studies suggest that it may have antioxidant and anti-inflammatory properties, but further research is needed to fully understand its potential therapeutic uses. Overall, (2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is a compound with diverse potential applications and is a subject of ongoing scientific investigation.

178738-48-2

Post Buying Request

178738-48-2 Suppliers

Recommended suppliers

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

178738-48-2 Usage

Uses

Used in Pharmaceutical Applications:
(2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is used as a pharmaceutical intermediate for the development of new drugs. Its potential biological activity, including antioxidant and anti-inflammatory properties, makes it a promising candidate for therapeutic applications.
Used in Research Applications:
(2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is used as a research tool to study its potential biological activity and therapeutic uses. It is a subject of ongoing scientific investigation to better understand its properties and potential applications in various fields.
Used in Antioxidant and Anti-Inflammatory Applications:
(2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is used as an antioxidant and anti-inflammatory agent in preclinical studies. Its potential to modulate these biological processes is being explored for the development of new treatments for various diseases and conditions.
Used in Drug Development:
(2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETAMIDE is used in drug development to create new pharmaceutical compounds with potential therapeutic benefits. Its unique structure and properties make it a valuable component in the design and synthesis of novel drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 178738-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,7,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 178738-48:
(8*1)+(7*7)+(6*8)+(5*7)+(4*3)+(3*8)+(2*4)+(1*8)=192
192 % 10 = 2
So 178738-48-2 is a valid CAS Registry Number.

178738-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-amoxilloic acid

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:178738-48-2 SDS

178738-48-2Upstream product

178738-48-2Downstream Products

178738-48-2Relevant academic research and scientific papers

Study of the Electroreactivity of Amoxicillin on Carbon Nanotube-Supported Metal Electrodes

Ferreira, Marta,Kuzniarska-Biernacka, Iwona,Fonseca, António M.,Neves, Isabel C.,Soares, Olívia S. G. P.,Pereira, Manuel F. R.,Figueiredo, José L.,Parpot, Pier

, p. 4914 - 4923 (2018/10/20)

The electroreactivity of amoxicillin (AMX) was studied on catalysts based on platinum, palladium and ruthenium supported on carbon nanotubes (Pt/CNT, Pd/CNT, Ru/CNT) in aqueous media using cyclic voltammetry. Cyclic voltammograms show two oxidation proces

Metal organic frameworks for selective degradation of amoxicillin in biomedical wastes

Paula, Marcos V.,Barros, Amanda L.,Wanderley, Kaline A.,De Sá, Gilberto F.,Eberlin, Marcos,Soares, Thereza A.,Alves, Severino Alves

, p. 2127 - 2136 (2018/09/29)

The accumulation of antibiotics in wastewater has led to the development and spreading of antibiotic resistance in the environment. Amoxicillin (Amox), a beta-lactamic antibiotic, is one of the most frequently consumed antibiotics in the world. We have applied two metal-organic frameworks (MOFs) containing zinc(II) as platforms to degrade Amox. We have predicted the adsorption of this antibiotic via molecular docking calculations which have been further corroborated by means of Fourier transform infrared and UV-Vis spectroscopies, thermogravimetric analysis, X-ray diffraction and scanning microscopy measurements. We have subsequently performed mass spectrometry analysis of Amox@zeolitic imidazolate framework-8 (ZIF-8) and Amox@Zn(1,4-benzenedicarboxylate) (ZnBDC) to demonstrate the degradation of Amox upon contact with the Zn-containing frameworks. We propose a possible pathway for the degradation of Amox involving the cleavage of the four-membered β-lactam ring. These Zn-containing frameworks provide a biocompatible platform for the degradation in solution of Amox, which should also be suitable to degrade other β-lactam antibiotics.

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 178738-48-2