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4-METHYL-5-THIAZOLEACETIC ACID, with the molecular formula C6H7NO2S, is a thiazole derivative characterized by its heterocyclic structure that includes both sulfur and nitrogen atoms. This chemical compound is recognized for its unique chemical structure and functional groups, which render it a versatile intermediate in the synthesis of a wide array of organic compounds. Its diverse reactivity and pharmacological properties position it as a promising candidate for the development of new medications and crop protection products.

5255-33-4

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5255-33-4 Usage

Uses

Used in Pharmaceutical Industry:
4-METHYL-5-THIAZOLEACETIC ACID is used as a building block for the synthesis of various drugs, leveraging its unique chemical structure to contribute to the development of new medications. Its potential applications in this industry are vast, given the compound's ability to react with a range of other molecules to form biologically active substances.
Used in Agricultural Industry:
In the agricultural sector, 4-METHYL-5-THIAZOLEACETIC ACID serves as a key intermediate in the production of agrochemicals. Its incorporation into the synthesis of crop protection products highlights its utility in enhancing agricultural yields and safeguarding crops from pests and diseases.
Given the compound's diverse applications, further research and development could potentially uncover additional uses across various industries, capitalizing on its reactivity and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5255-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5255-33:
(6*5)+(5*2)+(4*5)+(3*5)+(2*3)+(1*3)=84
84 % 10 = 4
So 5255-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2S/c1-4-5(2-6(8)9)10-3-7-4/h3H,2H2,1H3,(H,8,9)

5255-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methyl-1,3-thiazol-5-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 5-THIAZOLEACETIC ACID,4-METHYL

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:5255-33-4 SDS

5255-33-4Relevant academic research and scientific papers

Autocatalytic Oxidation of Thiamine Hydrochloride (Vitamin B1) by Permanganate in Aqueous Sulfuric Acid Medium: A Kinetic and Mechanistic Study

Savanur, Anita,Teradale, Amit,Lamani, Shekappa,Chimatadar, Shivamurti

, p. 281 - 291 (2016)

The reaction kinetics of autocatalytic oxidation of thiamine hydrochloride (vitamin B1) by the permanganate ion in aqueous sulfuric acid medium has been investigated spectrophotometrically under the pseudo-first-order condition at 25°C. The observed stoichiometry is 6:5 in terms of the mole ratio of permanganate ions and thiamine hydrochloride. Formation of products was confirmed by UV-vis, IR, GC-MS, and NMR spectral data. Usually in the permanganate oxidation-reduction reactions, one of the products, Mn2+ autocatalyzes the reaction, but in the present investigation the autocatalytic effect is due to the (4-methyl-thiazol-5-yl) acetic acid, a product formed from the oxidation of vitamin B1, which is a rare case. The added Mn2+ does not have any significant effect on the rate of reaction. The reaction is first order with respect to both permanganate and thiamine hydrochloride concentrations. An increase in the sulfuric acid concentration decreases the rate of reaction. A composite scheme and rate laws were proposed. The activation parameters with respect to the slow step and reaction constants involved in the mechanism were determined and discussed.

Synthesis method of 4-methylthiazole-5-formaldehyde

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Paragraph 0028; 0031-0033; 0036-0038; 0041-0043, (2021/05/01)

The invention provides a synthesis method of 4-methylthiazole-5-formaldehyde. The method comprises the following steps: 1) dissolving 4-methylthiazole-5-ethanol in a solvent, and carrying out oxidation reaction in the presence of a catalyst to obtain 4-methylthiazole-5-acetic acid; and 2) carrying out heating reaction on the 4-methylthiazole-5-acetic acid obtained in the step 1) in the presence of oxygen and a metal salt catalyst to obtain the 4-methylthiazole-5-formaldehyde. According to the method, 4-methylthiazole-5-ethanol is used as a raw material, the raw material is green, cheap and easy to obtain, the reaction process is mild in condition and environmentally friendly, the result selectivity is good, the yield is high, good economic benefits are achieved, and the method is suitable for industrial production.

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