CAS 5333-83-5
:1-(2-Thienyl)-1-butanone
Description:
1-(2-Thienyl)-1-butanone, with the CAS number 5333-83-5, is an organic compound characterized by its thienyl group, which is a five-membered aromatic ring containing sulfur. This compound features a butanone moiety, indicating the presence of a ketone functional group. It typically appears as a colorless to pale yellow liquid with a distinctive odor, often associated with its aromatic nature. The thienyl group contributes to its reactivity and potential applications in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. The compound is soluble in organic solvents, and its properties can be influenced by the presence of substituents on the thienyl ring. Additionally, 1-(2-Thienyl)-1-butanone may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken due to potential toxicity or reactivity.
Formula:C8H10OS
InChI:InChI=1/C8H10OS/c1-2-4-7(9)8-5-3-6-10-8/h3,5-6H,2,4H2,1H3
InChI key:InChIKey=YXHIINNJOGKPLF-UHFFFAOYSA-N
SMILES:C(CCC)(=O)C1=CC=CS1
Synonyms:- 1-(2-Thienyl)-1-butanone
- 1-(Thien-2-yl)butanone
- 1-(Thiophen-2-Yl)Butan-1-One
- 1-Butanone, 1-(2-thienyl)-
- 2-Butanoylthiophene
- 2-Butyrylthiophene
- 2-N-Butyrylthiophene
- Ketone, propyl 2-thienyl
- NSC 2350
- 1-Thien-2-ylbutan-1-one (2-Butanoylthiophene)
- Propyl 2-thienyl ketone
- N-PROPYL-2-THIENYL KETONE
- 1-(2-thienyl)butan-1-one
- 1-THIEN-2-YLBUTAN-1-ONE
- See more synonyms
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Found 5 products.
1-(Thiophen-2-yl)butan-1-one
CAS:Formula:C8H10OSPurity:97%Color and Shape:LiquidMolecular weight:154.22942-Butanoylthiophene
CAS:2-Butanoylthiophene is a com[ound of biochemical.Formula:C8H10OSColor and Shape:SolidMolecular weight:154.231-(2-Thienyl)-1-butanone
CAS:<p>1-(2-Thienyl)-1-butanone (1TBB) is a reactive oxygen species that has been shown to exhibit biological activity. 1TBB is an active oxygen species that can be used as a source of hydrogen peroxide, which is involved in the desulfurization of tobacco and the oxidation of ethylene to produce ethane. 1TBB also reacts with aliphatic aldehydes to form reactive intermediates, which may lead to oxidative injury. 1TBB has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>Formula:C8H10OSPurity:Min. 95%Molecular weight:154.04524




