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Morpholin-4-yl(oxo)acetic acid, a chemical compound with the molecular formula C7H11NO4, is a derivative of morpholine that features a carboxylic acid functional group and a ketone group. This unique structure positions it as a valuable building block in the synthesis of pharmaceutical drugs and drug candidates, making it a significant component in pharmaceutical research and development.

28911-34-4

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28911-34-4 Usage

Uses

Used in Pharmaceutical Research and Development:
Morpholin-4-yl(oxo)acetic acid is utilized as a key intermediate in the synthesis of pharmaceutical drugs and drug candidates. Its distinctive chemical structure allows for the development of innovative drug molecules, contributing to the advancement of treatments for various medical conditions.
Used in Organic Synthesis:
Beyond its pharmaceutical applications, morpholin-4-yl(oxo)acetic acid also serves as a crucial component in the field of organic synthesis. It is used as a precursor in the production of a variety of other chemical compounds, expanding its utility across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 28911-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,1 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28911-34:
(7*2)+(6*8)+(5*9)+(4*1)+(3*1)+(2*3)+(1*4)=124
124 % 10 = 4
So 28911-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO4/c8-5(6(9)10)7-1-3-11-4-2-7/h1-4H2,(H,9,10)

28911-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-morpholin-4-yl-2-oxoacetic acid

1.2 Other means of identification

Product number -
Other names morpholin-4-yl(oxo)acetic 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:28911-34-4 SDS

28911-34-4Downstream Products

28911-34-4Relevant academic research and scientific papers

Metal-, Photocatalyst-, and Light-Free Direct C-H Acylation and Carbamoylation of Heterocycles

Westwood, Matthew T.,Lamb, Claire J. C.,Sutherland, Daniel R.,Lee, Ai-Lan

, p. 7119 - 7123 (2019)

Direct C-H acylations and carbamoylations of heterocycles can now be readily achieved without requiring any conventional metal, photocatalyst, electrocatalysis, or light activation, thus significantly improving on sustainability, costs, toxicity, waste, and simplicity of the operational procedure. These mild conditions are also suitable for gram-scale reactions and late-stage functionalizations of complex molecules, including pharmaceuticals, N,N-ligands, and light-sensitive molecules.

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