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3-Ethoxy-5-methylisoxazole is an organic compound with the chemical formula C7H9NO2. It belongs to the isoxazole family, characterized by a five-membered ring containing oxygen and nitrogen atoms. The molecule features a methyl group and an ethoxy group attached to the isoxazole ring, providing it with both methyl and ethoxy substituents. This versatile and important chemical compound has a wide range of potential uses in various industries.

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  • 127020-20-6 Structure
  • Basic information

    1. Product Name: 3-ethoxy-5-Methylisoxazole
    2. Synonyms: 3-ethoxy-5-Methylisoxazole
    3. CAS NO:127020-20-6
    4. Molecular Formula: C6H9NO2
    5. Molecular Weight: 127.14116
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127020-20-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 203.6±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.040±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -2.60±0.50(Predicted)
    10. CAS DataBase Reference: 3-ethoxy-5-Methylisoxazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-ethoxy-5-Methylisoxazole(127020-20-6)
    12. EPA Substance Registry System: 3-ethoxy-5-Methylisoxazole(127020-20-6)
  • 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: 127020-20-6(Hazardous Substances Data)

127020-20-6 Usage

Uses

Used in Pharmaceutical Industry:
3-Ethoxy-5-methylisoxazole is used as a building block in organic synthesis for the production of pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-ethoxy-5-methylisoxazole is utilized as a building block in organic synthesis for the creation of agrochemicals. Its versatility allows for the development of various products used in agriculture to improve crop yields and protect plants from pests and diseases.
Used in Research and Development:
3-Ethoxy-5-methylisoxazole also has potential applications in research and development due to its distinctive structure and properties. It can be employed in the exploration of new chemical reactions, the synthesis of novel compounds, and the advancement of scientific knowledge in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 127020-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,2 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127020-20:
(8*1)+(7*2)+(6*7)+(5*0)+(4*2)+(3*0)+(2*2)+(1*0)=76
76 % 10 = 6
So 127020-20-6 is a valid CAS Registry Number.

127020-20-6SDS

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 3-Ethoxy-5-methyl-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 3-Ethoxy-5-methylisoxazole

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:127020-20-6 SDS

127020-20-6Relevant articles and documents

Synthesis of 3-ethoxyisoxazole derivatives and 3-ethoxy-1H-pyrazole derivatives from β-oxo thionoesters

Ohta,Fujisawa,Nakai,Furukawa

, p. 1861 - 1864 (2007/10/03)

3-Ethoxyisoxazoles and 3-ethoxy-1H-pyrazoles were obtained in high yields from β-oxo thionoesters. The reaction of the ethyl β-oxo thionoesters with hydroxylamine hydrochloride in the presence of triethylamine at room temperature for 2 h gave the ethyl 3-oxopropiohydroximates and their hemiacetals, which were easily converted to the 3-ethoxyisoxazoles by refluxing for 3 h at pH 3-5. On the other hand, the reaction of the ethyl β-oxo thionoesters with hydrazine derivatives in the presence of triethylamine for 3-8 h at room temperature directly yielded the 3-ethoxy-1H-pyrazoles.

Synthesis and single cell pharmacology of potential heterocyclic bioisosteres of the excitatory amino acid antagonist glutamic acid diethyl ester.

Madsen,Nielsen,Curtis,Beattie,Krogsgaard-Larsen

, p. 96 - 102 (2007/10/02)

A series of heterocyclic analogues of glutamic acid diethyl ester (GDEE), an antagonist at central excitatory amino acid receptors, have been synthesized and tested biologically. (RS)-Ethyl alpha-amino-alpha-(3-ethoxyisoxazol-5-yl)acetate (7), (RS)-ethyl

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