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1-(Thiophen-3-yl)butane-1,3-dione is an organic compound with the molecular formula C6H6O2S. It is a derivative of butane-1,3-dione, featuring a thiophene ring attached to the first carbon atom. Thiophene is a heterocyclic compound consisting of a benzene ring with one carbon atom replaced by a sulfur atom. 1-(Thiophen-3-yl)butane-1,3-dione is known for its potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as an intermediate in the preparation of dyes and pigments. Due to its unique structure, 1-(thiophen-3-yl)butane-1,3-dione exhibits interesting chemical properties and reactivity, making it a valuable building block in organic synthesis.

3115-63-7

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3115-63-7 Usage

Appearance

Yellow, crystalline substance

Odor

Distinctive, sweet

Usage

Flavoring agent in food and beverages

Applications

Production of pharmaceuticals and fragrances

Potential properties

Antioxidant and antimicrobial

Industries

Food and beverage, pharmaceuticals, and fragrances

Check Digit Verification of cas no

The CAS Registry Mumber 3115-63-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3115-63:
(6*3)+(5*1)+(4*1)+(3*5)+(2*6)+(1*3)=57
57 % 10 = 7
So 3115-63-7 is a valid CAS Registry Number.

3115-63-7Downstream Products

3115-63-7Relevant academic research and scientific papers

Palladium-catalysed carbonylative α-arylation of acetone and acetophenones to 1,3-diketones

Schranck, Johannes,Tlili, Anis,Alsabeh, Pamela G.,Neumann, Helfried,Stradiotto, Mark,Beller, Matthias

supporting information, p. 12624 - 12628 (2013/10/01)

Three COmponent α-arylation: A carbonylative ketone α-arylation process employing acetone for the first time, as well as acetophenones, is described (see scheme). The reaction tolerates a range of (hetero)aryl iodides and several functionalised aryl ketone coupling partners. Only low pressures of molecular CO are applied and no additional solvent is necessary. Copyright

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