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Ethyl 2-methoxyisonicotinate, a chemical compound with the formula C10H13NO4, is a derivative of isonicotinic acid featuring a methoxy group. It is recognized for its potential medicinal properties and is a valuable compound in the field of medicinal chemistry due to its anti-inflammatory, antioxidant, and anti-cancer properties.

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  • 105596-61-0 Structure
  • Basic information

    1. Product Name: Ethyl 2-methoxyisonicotinate
    2. Synonyms: Ethyl 2-methoxyisonicotinate
    3. CAS NO:105596-61-0
    4. Molecular Formula: C9H11NO3
    5. Molecular Weight: 181.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105596-61-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 254.5 °C at 760 mmHg
    3. Flash Point: 107.7 °C
    4. Appearance: white crystalline power
    5. Density: 1.124 g/cm3
    6. Vapor Pressure: 0.0172mmHg at 25°C
    7. Refractive Index: 1.5
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: Ethyl 2-methoxyisonicotinate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethyl 2-methoxyisonicotinate(105596-61-0)
    12. EPA Substance Registry System: Ethyl 2-methoxyisonicotinate(105596-61-0)
  • 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: 105596-61-0(Hazardous Substances Data)

105596-61-0 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 2-methoxyisonicotinate is used as a potential drug candidate for the treatment of various diseases and conditions, leveraging its anti-inflammatory, antioxidant, and anti-cancer properties to address a range of health issues.
Used in Medicinal Chemistry Research:
It is utilized as a subject of study for its chemical structure and properties, contributing to the advancement of knowledge and the development of new therapeutic agents in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 105596-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105596-61:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*6)+(2*6)+(1*1)=130
130 % 10 = 0
So 105596-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-3-13-9(11)7-4-5-10-8(6-7)12-2/h4-6H,3H2,1-2H3

105596-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-methoxyisonicotinate

1.2 Other means of identification

Product number -
Other names ethyl 2-methoxypyridine-4-carboxylate

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:105596-61-0 SDS

105596-61-0Relevant articles and documents

Chemical compounds

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Example 62, (2010/11/29)

The invention relates to quinazoline derivatives of the formula: [wherein: Y1represents —O—, —S—, —CH2—, —SO—, —SO2—, —NR5CO—, —CONR6—, —SO2NR7—, —NR8SO2— or —NR9— (wherein R5, R6, R8and R9each independently represents hydrogen, alkyl or alkoxyalkyl); R1represents hydrogen, hydroxy, halogeno, nitro, trifluoromethyl, cyano, alkyl, alkoxy, alkylthio, amino or alkylamino. R2represents hydrogen, hydroxy, halogeno, alkyl, alkoxy, trifluoromethyl, cyano, amino or nitro; m is an integer from 1 to 5; R3represents hydroxy, halogeno, alkyl, alkoxy, alkanoyloxy, trifluoromethyl, cyano, amino or nitro; R4represents a group which is or which contains an optionally substituted pyridone, phenyl or aromatic heterocyclic group] and salts thereof; processes for their preparation and pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.

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