1468-83-3 | 3-Acetylthiophene

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$6.00	$4.00
5g	98%	in stock	$15.00	$11.00
10g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$50.00	$35.00
100g	98%	in stock	$196.00	$137.00

Description

• Catalog Number: AA65054
• Chemical Name: 3-Acetylthiophene
• CAS Number: 1468-83-3
• Molecular Formula: C6H6OS
• Molecular Weight: 126.1762
• MDL Number: MFCD00005468
• SMILES: CC(=O)c1cscc1

Computed Properties

• Complexity: 101
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

3-Acetylthiophene is a versatile compound widely used in chemical synthesis for its unique properties and applications. As a key building block in organic chemistry, 3-Acetylthiophene plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. One of the main applications of 3-Acetylthiophene is its utilization as a precursor in the synthesis of heterocyclic compounds. By reacting with different reagents and catalysts, 3-Acetylthiophene can undergo various functional group transformations, enabling the formation of diverse chemical structures with desirable properties.Furthermore, 3-Acetylthiophene is often employed in the preparation of flavor and fragrance compounds due to its sulfur-containing moiety, which can contribute unique aromatic notes to the final products. This makes it a valuable ingredient in the production of perfumes, food additives, and other aromatic substances.Overall, the versatility and reactivity of 3-Acetylthiophene make it an indispensable tool for synthetic chemists seeking to create complex molecular structures with specific functionalities for a wide range of industrial applications.

Literature

• 1-(Thiophen-3-yl)ethanone.

  Acta crystallographica. Section C, Crystal structure communications 20110601

• Transition metal catalyzed manipulation of non-polar carbon-hydrogen bonds for synthetic purpose.

  Proceedings of the Japan Academy. Series B, Physical and biological sciences 20110511

• A poly(3-acetylthiophene) modified glassy carbon electrode for selective voltammetric measurement of uric acid in urine sample.

  Chemical & pharmaceutical bulletin 20080301

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601