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(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is a chemical compound with the molecular formula C12H15NO6, characterized as a yellow crystalline solid. It is an ester derivative of (4,5-dimethoxy-2-nitrophenyl)acetic acid, featuring two methoxy groups, a nitro group, and an ethyl ester group. (4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is recognized for its potent antioxidant and anti-inflammatory properties, and it has demonstrated potential in treating a range of diseases, including cancer, asthma, and rheumatoid arthritis. Its diverse biological activities and potential therapeutic applications make it a valuable compound in research settings.

5415-53-2

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5415-53-2 Usage

Uses

Used in Pharmaceutical Industry:
(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals due to its versatile chemical structure and biological activities. Its antioxidant and anti-inflammatory properties contribute to the development of drugs for treating a variety of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, (4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER serves as an intermediate in the synthesis of agrochemicals, potentially contributing to the development of new pesticides or other agricultural products that can enhance crop protection and yield.
Used in Antioxidant Applications:
(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is utilized as a potent antioxidant, protecting cells from oxidative stress and damage, which is crucial in the development of treatments for various diseases where oxidative stress plays a significant role.
Used in Anti-Inflammatory Applications:
(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is employed as an anti-inflammatory agent, helping to reduce inflammation which is a common factor in many diseases such as asthma and rheumatoid arthritis, thereby contributing to the development of therapeutics for these conditions.
Used in Cancer Treatment Research:
(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID ETHYL ESTER is used in research for its potential role in cancer treatment, as it has shown promise in targeting various aspects of cancer cell behavior, including proliferation and survival.

Check Digit Verification of cas no

The CAS Registry Mumber 5415-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5415-53:
(6*5)+(5*4)+(4*1)+(3*5)+(2*5)+(1*3)=82
82 % 10 = 2
So 5415-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO6/c1-4-19-12(14)6-8-5-10(17-2)11(18-3)7-9(8)13(15)16/h5,7H,4,6H2,1-3H3

5415-53-2SDS

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 ethyl 2-(4,5-dimethoxy-2-nitrophenyl)acetate

1.2 Other means of identification

Product number -
Other names benzeneacetic acid,4,5-dimethoxy-2-nitro-,ethyl ester

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:5415-53-2 SDS

5415-53-2Relevant academic research and scientific papers

NURR1 RECEPTOR MODULATORS

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Paragraph 0646; 1213; 1216-1217, (2020/09/08)

Described herein, inter alia, are Nurr1 receptor modulators and uses thereof. In an aspect is provided a method for treating a disease associated with dysregulation and/or degeneration of dopaminergic neurons in the central nervous system of a subject in need thereof, the method including administering to the subject in need thereof a therapeutically effective amount of a compound described herein.

1,2-disubstituted-6-oxo-3-phenyl-piperidine-3-carboxamides and combinatorial libraries thereof

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, (2008/06/13)

The invention relates to combinatorial libraries containing two or more novel piperidine-3-carboxamide derivative compounds, methods of preparing the piperidine-3-carboxamide derivative compounds and piperidine-3-carboxamide derivative compounds bound to a resin

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