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2-(dimethoxymethyl)quinoxaline 1,4-dioxide is an organic compound with the molecular formula C10H12N2O4. It is a derivative of quinoxaline, which is a heterocyclic compound consisting of a six-membered aromatic ring containing carbon and nitrogen atoms. The presence of two methoxymethyl groups attached to the 2nd carbon and the 1,4-dioxide functional group gives this compound unique properties and potential applications in various fields.

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  • 32065-66-0 Structure
  • Basic information

    1. Product Name: 2-(dimethoxymethyl)quinoxaline 1,4-dioxide
    2. Synonyms: 2-(dimethoxymethyl)quinoxaline 1,4-dioxide;2-(DIMETHOXYMETHYL)CHINOXALINE-1,4-DIOXIDE
    3. CAS NO:32065-66-0
    4. Molecular Formula: C11H12N2O4
    5. Molecular Weight: 236.22398
    6. EINECS: 250-910-9
    7. Product Categories: N/A
    8. Mol File: 32065-66-0.mol
    9. Article Data: 2
  • 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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(dimethoxymethyl)quinoxaline 1,4-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(dimethoxymethyl)quinoxaline 1,4-dioxide(32065-66-0)
    11. EPA Substance Registry System: 2-(dimethoxymethyl)quinoxaline 1,4-dioxide(32065-66-0)
  • 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: 32065-66-0(Hazardous Substances Data)

32065-66-0 Usage

Uses

Used in Pharmaceutical Industry:
2-(dimethoxymethyl)quinoxaline 1,4-dioxide is used as an intermediate in the synthesis of Cyadox, which is an antibiotic drug. 2-(dimethoxymethyl)quinoxaline 1,4-dioxide plays a crucial role in the development of new antibiotics to combat bacterial infections.
Used in Animal Feed Industry:
2-(dimethoxymethyl)quinoxaline 1,4-dioxide has the potential to be used as a feedstuff additive in promoting the growth of animals. Its incorporation into animal feed can enhance the overall health and productivity of livestock, contributing to the efficiency of the animal feed industry.

Check Digit Verification of cas no

The CAS Registry Mumber 32065-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,6 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32065-66:
(7*3)+(6*2)+(5*0)+(4*6)+(3*5)+(2*6)+(1*6)=90
90 % 10 = 0
So 32065-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O4/c1-16-11(17-2)10-7-12(14)8-5-3-4-6-9(8)13(10)15/h3-7,11H,1-2H3

32065-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethoxymethyl)-4-oxidoquinoxalin-1-ium 1-oxide

1.2 Other means of identification

Product number -
Other names quinoxaline-di-N-oxide-2-carboxyaldehyde dimethylacetal

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:32065-66-0 SDS

32065-66-0Relevant articles and documents

Quinoxaline - 1, 4 - dioxide in animal use in the manufacture of

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Paragraph 0081; 0082; 0083, (2017/07/01)

The invention discloses an antibacterial derivative of a quinoxaline-1,4-dioxide and application of the antibacterial derivative in animal production. The derivative of the quinoxaline-1,4-dioxide as shown in a formula 1, a formula 2, a formula 3, a formula 4, a formula 5 or a formula 6 or a salt of the derivative has excellent antibacterial activity, is low-toxic or non-toxic to livestock, and has higher antibacterial activity and higher safety than the existing quinoxaline derivative products in the market, and therefore, the derivative of the quinoxaline-1,4-dioxide or the salt of the derivative can be used as a growth promoter for a feed to promote the growth of the livestock, and has excellent application prospect in the breeding industry.

Synthesis and Biological Evaluation of New Quinoxaline Derivatives as Antioxidant and Anti-Inflammatory Agents

Burguete, Asuncion,Pontiki, Eleni,Hadjipavlou-Litina, Dimitra,Ancizu, Saioa,Villar, Raquel,Solano, Beatriz,Moreno, Elsa,Torres, Enrique,Perez, Silvia,Aldana, Ignacio,Monge, Antonio

scheme or table, p. 255 - 267 (2012/01/13)

We report the synthesis, anti-inflammatory, and antioxidant activities of novel quinoxaline and quinoxaline 1,4-di-N-oxide derivatives. Microwave-assisted methods have been used to optimize reaction times and to improve yields. The tested compounds presented important scavenging activities and promising in vitro inhibition of soybean lipoxygenase (LOX). Two of the best LOX inhibitors (compounds 7b and 8f) were evaluated as invivo anti-inflammatory agents using the carrageenin-induced edema model. One of them (compound 7b) showed important in vivo anti-inflammatory effect (41%) similar to that of indomethacin (47%) used as the reference drug. Synthesis and Biological Evaluation of New Quinoxaline Derivatives as Antioxidant and Anti-Inflammatory Agents Asuncion Burguete, Eleni Pontiki, Dimitra Hadjipavlou-Litina*, Saioa Ancizu, Raquel Villar, Beatriz Solano, Elsa Moreno, Enrique Torres, Silvia Perez, Ignacio Aldana and Antonio Monge The synthesis, anti-inflammatory and antioxidant activities of new quinoxaline derivatives are reported. The new compounds exhibit important scavenging activities and promising values of in vitro inhibition of soybean LOX, One of them shows strong in vivo anti-inflammatory effect similar to that of indomethacin used as the reference drug.

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