2-Methylthiazoline is a heterocyclic compound that has been studied for its potential applications in various fields, including:
- **Synthesis:** 2-Methylthiazoline can be synthesized through several methods, including the reaction of 2-aminoethanethiol with an aldehyde or ketone.
- **Biological Activity:** 2-Methylthiazoline has been shown to possess antibacterial activity against a variety of bacterial strains. It has also been investigated for its potential as a flavoring agent in food products.
- **Importance:** The compound is of interest due to its sulfur-containing heterocyclic ring structure, which often contributes to biological activity.
- **Research:** Researchers study 2-methylthiazoline to explore its potential as a lead compound for the development of new drugs and food additives. It's also investigated for its potential role in various biological processes and its contribution to the aroma of certain foods.
- **Other:** It is a volatile compound with a characteristic odor.'
ID Source | ID |
---|---|
PubMed CID | 16867 |
CHEBI ID | 184712 |
SCHEMBL ID | 208968 |
MeSH ID | M0085537 |
Synonym |
---|
LS-12993 |
2-thiazoline, 2-methyl- |
thiazole, 4,5-dihydro-2-methyl- |
2-methyl-4,5-dihydrothiazole |
inchi=1/c4h7ns/c1-4-5-2-3-6-4/h2-3h2,1h |
2-methyl-2-thiazoline, 98% |
methyl-2-thiazoline |
brn 0104274 |
4,5-dihydro-2-methylthiazole |
methyl-2 delta-2 thiazoline [french] |
2-methyl-2-thiazoline |
2-methylthiazoline |
einecs 219-071-6 |
2346-00-1 |
M0285 |
2-methyl-4,5-dihydro-1,3-thiazole |
CHEBI:184712 |
AKOS000120137 |
methyl-2 delta-2 thiazoline |
4-27-00-00921 (beilstein handbook reference) |
unii-8z6ua8v7wn |
8z6ua8v7wn , |
A816733 |
c4h7ns |
FT-0613088 |
SCHEMBL208968 |
2-methyl-4,5-dihydro-1,3-thiazole # |
AKOS025243234 |
DTXSID1062336 |
W-107400 |
2-methyl-.delta.2-thiazoline |
mfcd00005314 |
2-methyl-2-thiazoline, analytical standard |
4,5-dihydro-2-methyl-thiazole |
2-methyl-laquo deltaraquo 2-thiazoline |
2-methyl-2-thiazoline, 8ci |
F0001-0813 |
2-methyl-4,5-dihydro-thiazole |
AMY23228 |
EN300-20730 |
Q27271229 |
D91305 |
CS-W013704 |
Z104480256 |
Class | Description |
---|---|
thiazoles | An azole in which the five-membered heterocyclic aromatic skeleton contains a N atom and one S atom. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (14.29) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 4 (57.14) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (13.21) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 7 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |