Welcome to LookChem.com Sign In|Join Free
  • or
2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid is a heterocyclic chemical compound that belongs to the class of oxathiine carboxylic acids. It features a six-membered ring structure with one oxygen and one sulfur atom, along with a methyl group and a carboxylic acid functional group.

6577-69-1

Post Buying Request

6577-69-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6577-69-1 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals. Its unique molecular structure and functional groups make it a valuable component in the development of new drugs.
Used in Agrochemical Synthesis:
2-methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid is also utilized in the synthesis of agrochemicals, contributing to the development of pesticides and other agricultural products that can enhance crop protection and yield.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, 2-methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid is used as an active ingredient in antimicrobial agents, helping to combat bacterial infections.
Used in Antiviral Applications:
2-methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid's antiviral properties make it a potential candidate for the development of antiviral drugs, which can be crucial in treating viral infections and diseases.
Used in Organic Synthesis Research:
2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid serves as a key intermediate in organic synthesis, facilitating the creation of complex organic molecules for various applications in research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 6577-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6577-69:
(6*6)+(5*5)+(4*7)+(3*7)+(2*6)+(1*9)=131
131 % 10 = 1
So 6577-69-1 is a valid CAS Registry Number.

6577-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2,3-dihydro-1,4-oxathiine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-5,6-dihydro-1,4-oxathiin-3-carboxylic acid

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:6577-69-1 SDS

6577-69-1Relevant academic research and scientific papers

Studies on the Preparation of Dihydro-1,4-oxathiines. Computer-Assisted Evaluation of the Results of Retrosynthetic Analysis Verified by Synthetic Experiments and By-Product Analyses. Synthetic Pathways Involving α-Sulfenylated Ketones and 1,3-Oxathiolanes of α-Halo and α-Hydroxy K...

Nevalainen, Vesa,Pohjala, Esko,Maelkoenen, Pentti,Hukkanen, Heikki

, p. 591 - 602 (2007/10/02)

The preparation of 2- and 2,3-substituted 5,6-dihydro-1,4-oxathiines has been studied by computer simulation and by experiment.Three major synthetic pathways, involving 2-(1-hydroxyalkyl)-1,3-oxathiolanes, 2-(1-haloalkyl)-1,3-oxathiolanes, 2-hydroxyethylthiomethyl ketones, methanesulfonates of 2-hydroxyethylthiomethyl ketones and 2-choroethylthiomethyl ketones as intermediates, were evaluated, by running the program CAMEO, and by experiment.The results of the two approaches were compared and the major by-products of the reactions were identified by GLC/MS.

Studies on the Formation of Dihydro-1,4-oxathiines by Halogenation of 1,3-Oxathiolanes.

Nevalainen, Vesa,Pohjala, Esko

, p. 1401 - 1421 (2007/10/02)

Formation of 5,6-dihydro-1,4-oxathiines (1a-g) by halogenation of 1,3-oxathiolanes (4a-g) was investigated.Moderate yields of (1) were obtained in systems in which the newly formed double bond of the heterocyclic ring was stabilised by conjugation.In addition to the dihydro-1,4-oxathiines (1a-g), their halogenated derivatives and some fused and spiro 1,4-oxathianes were produced as by-products.By-products of reactions were analysed by gas chromatography and mass-spectrometry.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6577-69-1