2689-70-5 Usage
Uses
Due to the limited information available on Methyl 2-Methyl-3-Oxo-Tetrahydrothiophene-2-Carbonate, its uses are not well-defined. However, based on the general properties of tetrahydrothiophenes, it can be speculated that Methyl 2-Methyl-3-Oxo-Tetrahydrothiophene-2-Carbonate may have potential applications in various industries. Some possible uses could include:
Used in Pharmaceutical Industry:
Methyl 2-Methyl-3-Oxo-Tetrahydrothiophene-2-Carbonate could be used as an intermediate in the synthesis of pharmaceutical compounds, given its unique structure and the presence of a sulfur atom, which is often found in biologically active molecules.
Used in Chemical Synthesis:
Methyl 2-Methyl-3-Oxo-Tetrahydrothiophene-2-Carbonate may serve as a building block or a reagent in the synthesis of more complex organic molecules, particularly those containing sulfur atoms, which are common in various chemical and pharmaceutical applications.
Used in Material Science:
Methyl 2-Methyl-3-Oxo-Tetrahydrothiophene-2-Carbonate could potentially be used in the development of new materials with unique properties, such as improved thermal stability or chemical resistance, due to the presence of the sulfur atom in its structure.
Check Digit Verification of cas no
The CAS Registry Mumber 2689-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2689-70:
(6*2)+(5*6)+(4*8)+(3*9)+(2*7)+(1*0)=115
115 % 10 = 5
So 2689-70-5 is a valid CAS Registry Number.
2689-70-5Relevant academic research and scientific papers
Regioselective synthesis of methyl 3-thiothiophene-2-carboxylate derivatives utilizing a dehydration-type ti-dieckmann condensation
Nagase, Ryohei,Gotoh, Hideki,Katayama, Mayumi,Manta, Naoki,Tanabe, Yoo
, p. 697 - 708 (2008/03/13)
Regioselective dehydration-type Ti-Dieckmann condensation of 3-(methoxycarbonylmethylthio)propanethioates successfully afforded methyl thiophene-2-carboxylates and methyl 4,5-dihydrothiophene-2-carboxylates, utilizing TiCl4 - Et3N an
