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N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is a chemical compound with the molecular formula C11H15N3O. It is a pyridine derivative that has garnered interest in pharmaceutical research and drug development due to its potential therapeutic applications. N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide is recognized for its ability to modulate biological processes and has shown promise in preclinical studies for addressing a range of medical conditions.

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  • 90873-00-0 Structure
  • Basic information

    1. Product Name: N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide
    2. Synonyms: N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide
    3. CAS NO:90873-00-0
    4. Molecular Formula: C10H14N2O
    5. Molecular Weight: 178.23096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90873-00-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide(90873-00-0)
    11. EPA Substance Registry System: N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide(90873-00-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 90873-00-0(Hazardous Substances Data)

90873-00-0 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is utilized as a research compound for exploring its potential role in treating various medical conditions. Its unique structure and properties make it a valuable candidate for further investigation into its therapeutic effects.
Used in Neurodegenerative Disease Treatment:
In the field of neurology, N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is used as a potential therapeutic agent for neurodegenerative diseases. Its ability to modulate biological processes suggests it may have applications in managing or treating conditions such as Alzheimer's disease, Parkinson's disease, and other related disorders.
Used in Cancer Treatment:
Oncology research has also focused on N-(5-ethyl-2-Methylpyridin-4-yl)acetamide as a potential anticancer agent. Its capacity to interact with biological targets makes it a candidate for further study in the development of treatments for various types of cancer.
Used in Anti-Inflammatory Applications:
In the realm of inflammation and immune response, N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is considered for its potential as an anti-inflammatory agent. It may be used to study and develop treatments for conditions characterized by excessive or chronic inflammation.
Used as a Building Block in Organic Synthesis:
Beyond its direct therapeutic applications, N-(5-ethyl-2-Methylpyridin-4-yl)acetamide also serves as a key building block in organic synthesis. It is used to create other pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 90873-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90873-00:
(7*9)+(6*0)+(5*8)+(4*7)+(3*3)+(2*0)+(1*0)=140
140 % 10 = 0
So 90873-00-0 is a valid CAS Registry Number.

90873-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-ethyl-2-methylpyridin-4-yl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Acetamino-2-methyl-5-ethyl-pyridin

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:90873-00-0 SDS

90873-00-0Relevant articles and documents

Improved Synthesis of N1-Pyridylthiamine Pyrophosphate, a Coenzymatically Active Analog of Thiamine Pyrophosphate

Neef, Holger,Golbik, Ralph,Fahlbusch, Baerbel,Schellenberger, Alfred

, p. 913 - 916 (2007/10/02)

Our previously published synthesis of the N1-pyridyl analog 1b of thiamine pyrophosphate is improved resulting in a remarkably higher yield.Key reaction of this new synthetic pathway is the oxidative degradation of 5-acetylpyridine 8 to the 5-carboxylic acid 11 via the pyridinium compound 10.Improved preparations of other intermediates are also described.The N1-pyridylthiamine pyrophosphate analog 1b has been separated and purified by ion exchange chromatography on Sephadex A-25.

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