What is the 4-ethyl-2-methyl-4,5-dihydrothiazole?

4-ethyl-2-methyl-4,5-dihydrothiazole is , while it's Molecular Formula is C6H11 N S. Due to the limited information available on 4-ethyl-2-methyl-4,5-dihydrothiazole, its specific applications cannot be accurately listed. However, based on its chemical structure and properties, it may potentially be used in various industries such as pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other organic compounds. Further research and development are required to explore its potential applications and establish appropriate safety measures for its use.

What is the CAS number for 4-ethyl-2-methyl-4,5-dihydrothiazole?

The CAS number of 4-ethyl-2-methyl-4,5-dihydrothiazole is 4293-61-2.

What is 4-ethyl-2-methyl-4,5-dihydrothiazole (4293-61-2) used for?

4-Ethyl-2-methyl-4,5-dihydrothiazole is a chemical compound belonging to the class of organic compounds known as thiazolines. It is a heterocyclic compound with a five-membered ring containing three carbon atoms, one nitrogen atom, and one sulfur atom. The molecular structure of 4-ethyl-2-methyl-4,5-dihydrothiazole features a thiazoline ring with ethyl and methyl substituents at positions 4 and 2, respectively. It is sparingly soluble in water. However, information about its production, uses, toxicity, or other specific properties is not widely available, necessitating further evaluation of its application and safety measures.InChI:InChI=1/C6H11NS/c1-3-6-4-8-5(2)7-6/h6H,3-4H2,1-2H3

What is the 4-ethyl-2-methyl-4,5-dihydrothiazole?

4-ethyl-2-methyl-4,5-dihydrothiazole is , while it's Molecular Formula is C6H11 N S. Due to the limited information available on 4-ethyl-2-methyl-4,5-dihydrothiazole, its specific applications cannot be accurately listed. However, based on its chemical structure and properties, it may potentially be used in various industries such as pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other organic compounds. Further research and development are required to explore its potential applications and establish appropriate safety measures for its use.

What is the CAS number for 4-ethyl-2-methyl-4,5-dihydrothiazole?

The CAS number of 4-ethyl-2-methyl-4,5-dihydrothiazole is 4293-61-2.

What is 4-ethyl-2-methyl-4,5-dihydrothiazole (4293-61-2) used for?

4-Ethyl-2-methyl-4,5-dihydrothiazole is a chemical compound belonging to the class of organic compounds known as thiazolines. It is a heterocyclic compound with a five-membered ring containing three carbon atoms, one nitrogen atom, and one sulfur atom. The molecular structure of 4-ethyl-2-methyl-4,5-dihydrothiazole features a thiazoline ring with ethyl and methyl substituents at positions 4 and 2, respectively. It is sparingly soluble in water. However, information about its production, uses, toxicity, or other specific properties is not widely available, necessitating further evaluation of its application and safety measures.InChI:InChI=1/C6H11NS/c1-3-6-4-8-5(2)7-6/h6H,3-4H2,1-2H3

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4-ethyl-2-methyl-4,5-dihydrothiazole

CAS No.: 4293-61-2
Purity: 99%

Manufacturer supply good quality 4-ethyl-2-methyl-4,5-dihydrothiazole 4293-61-2 with stock

Molecular Formula: C6H11 N S
Molecular Weight: 129.226
Vapor Pressure: 1.98mmHg at 25°C
Refractive Index: 1.4980-1.5010
Boiling Point: 170.1°Cat760mmHg
Flash Point: 56.7°C
PSA： 37.66000
Density: 1.09g/cm³
LogP: 1.36580

4-ethyl-2-methyl-4,5-dihydrothiazole(Cas 4293-61-2) Usage

General Description

4-Ethyl-2-methyl-4,5-dihydrothiazole is a chemical compound that belongs to the class of organic compounds known as thiazolines, which are heterocyclic compounds with a five-member ring containing three carbon atoms, one nitrogen atom, and one sulfur atom. These are satuated compounds that are a derivative of thiazole. The detailed molecular structure of this chemical consists of a thiazoline ring bearing ethyl and methyl substituents at positions 4 and 2 respectively. It is sparingly soluble in water. Information about the production, uses, toxicity or other specific properties of 4-ethyl-2-methyl-4,5-dihydrothiazole are not widely available, therefore its application and safety measures should be evaluated further.

InChI:InChI=1/C6H11NS/c1-3-6-4-8-5(2)7-6/h6H,3-4H2,1-2H3

4293-61-2 Relevant articles

Generation of cyclic ketene-N,X-acetals (X = O, S) from 2-alkyl-1,3-oxazolines and 2-alkyl-1,3-thiazolines. Reactions with acid chlorides, 1,3-diacid chlorides and N-(chlorocarbonyl) isocyanate

Zhou, Aihua,Pittman Jr., Charles U.

, p. 37 - 48 (2007/10/03)

2-Alkyl-1,3-oxazolines, 2-alkyl-1,3-thia...

Reactions of 2-methylthiazolines and N-methyl cyclic ketene-N,S-acetals with acid chlorides

Zhou, Aihua,Pittman, Charles U.

, p. 8899 - 8903 (2007/10/03)

Carbon-carbon bond formation occurs unde...

Synthesis and absolute configuration of chain branched cimetidine analogous thioethers

Elz,Drager,Schunack

, p. 348 - 354 (2007/10/02)

Potential antiradiation drugs. II. 2-Amino-1-alkanethiols, 1-amino-2-alkanethiols, 2-thiazolines, and 2-thiazoline-2-thiols.

Handrick,Atkinson,Granchelli,Bruni

, p. 762 - 766 (2007/10/04)

4293-61-2 Process route

: 96-20-8,13054-87-0
2-aminobutanol

: 75-36-5
acetyl chloride

: 4293-61-2
4-ethyl-2-methylthiazoline

Conditions

Conditions	Yield
2-aminobutanol; acetyl chloride; With triethylamine; In dichloromethane; at 0 ℃; for 0.5h; With Lawessons reagent; In toluene; for 0.25h; Further stages.; Heating;