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2-oxo-1,3-oxazolidine-4-carboxylic acid (SALTDATA: FREE) is a white crystalline chemical compound with the molecular formula C4H5NO4 and a molar mass of 131.09 g/mol. It belongs to the oxazolidine carboxylic acid family and is known for its versatile applications in various chemical reactions, synthesis processes, and industries.

89033-27-2

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89033-27-2 Usage

Uses

Used in Pharmaceutical Industry:
2-oxo-1,3-oxazolidine-4-carboxylic acid (SALTDATA: FREE) is used as a building block in organic synthesis for the development of pharmaceutical compounds. Its unique structure and functional groups make it a valuable component in the synthesis of various drug molecules, contributing to the discovery of new therapeutic agents.
Used in Agricultural Industry:
In the agricultural sector, 2-oxo-1,3-oxazolidine-4-carboxylic acid (SALTDATA: FREE) serves as a chelating agent in metal complexation reactions. This property allows it to form stable complexes with metal ions, which can be utilized in the development of agrochemicals, such as fertilizers and pesticides, to improve their efficiency and reduce environmental impact.
Used in Chemical Reactions and Synthesis Processes:
2-oxo-1,3-oxazolidine-4-carboxylic acid (SALTDATA: FREE) is employed as a versatile reagent in various chemical reactions and synthesis processes. Its ability to participate in a wide range of reactions, such as esterification, amidation, and condensation, makes it a valuable tool for chemists in the synthesis of complex organic molecules and the development of new materials.
Potential Biological and Pharmacological Activities:
2-oxo-1,3-oxazolidine-4-carboxylic acid (SALTDATA: FREE) may also possess biological and pharmacological activities, making it a subject of interest for further research and development. Its potential applications in this area could include the development of new drugs, therapeutic agents, or diagnostic tools, based on its unique chemical properties and interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 89033-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89033-27:
(7*8)+(6*9)+(5*0)+(4*3)+(3*3)+(2*2)+(1*7)=142
142 % 10 = 2
So 89033-27-2 is a valid CAS Registry Number.

89033-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Oxo-1,3-oxazolidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Oxazolidinecarboxylic acid,2-oxo

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:89033-27-2 SDS

89033-27-2Relevant academic research and scientific papers

Synthesis method of multi-configuration 2-oxooxazolidine-4-carboxylic acid compound

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Paragraph 0048-0050; 0052-0055, (2020/11/01)

The invention relates to a synthesis method of a multi-configuration 2-oxooxazolidine-4-carboxylic acid compound, wherein the synthesis method comprises the following steps: (1) under the protection of inert gas, carrying out a reaction on a compound represented by a formula I or an isomer thereof with S,S'-dimethyl dithiocarbonate in the presence of water to obtain a compound represented by a formula II or an isomer thereof; (2) carrying out hydrolysis reaction on the compound represented by the formula II or the isomer thereof under an alkaline condition to prepare a compound represented bya formula III or an isomer thereof, wherein the structural formula of the compound represented by the formula I is shown in the specification, the structural formula of the compound represented by theformula II is shown in the specification, the structural formula of the compound represented by the formula III is shown in the specification, in the formula I, the formula II and the formula III, Ris one of H and alkyl with 1-5 carbon atoms. According to the method, water is used as a solvent, so that the method is green, environment-friendly, high in safety, easy in reaction operation and easyin reaction condition control, and the product yield is up to 86% or above.

Quinoline-based compound and selective androgen receptor agonist comprising the same

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Paragraph 0248-0250, (2016/10/08)

Provided are a novel quinoline-based compound, a pharmaceutical composition containing the quinoline-based compound, and a method for producing the quinoline-based compound. The quinoline-based compound acts on an androgen receptor to increase activities of the androgen receptor, and thus can be favorably used as an agent for treating and preventing diseases or conditions, in which the increased activities of the androgen can lead to improvement of symptoms or the responsiveness to treatment, for example, various hormone-related diseases of the male or female, muscle-wasting disease, osteoporosis, and the like.COPYRIGHT KIPO 2016

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