3-Acetyl-2,5-dimethylthiophene, 99%
3-Acetyl-2,5-dimethylthiophene, 99%
Thermo Scientific Chemicals

3-Acetyl-2,5-dimethylthiophene, 99%

CAS: 2530-10-1 | C9H22O3Si | 206.36 g/mol
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Catalog NumberQuantity
ALFA17329.0910 g
Catalog number ALFA17329.09
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Quantity:
10 g
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Specifications
Chemical Name or Material3-Acetyl-2,5-dimethylthiophene
CAS2530-10-1
Health Hazard 1Warning
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3GHS P Statement
P261-P280-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapors/spray.
Wear protective gloves/protective clothing/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.
Store locked up.
Dispose of contents/container in accordance with local/regional/national/international regulations.
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It is used in the synthesis of heterocyclic ketimines, 3-acetyl-2,5-dimethylthiophene thiosemicarbazone and 3-acetyl-2,5- dimethylthiophene semicarbazone.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used in the synthesis of heterocyclic ketimines, 3-acetyl-2,5-dimethylthiophene thiosemicarbazone and 3-acetyl-2,5- dimethylthiophene semicarbazone.

Solubility
Soluble in alcohol. Insoluble in water.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Krishna Sharma, et. al. Microwave assisted synthesis, characterization and biological evaluation of palladium and platinum complexes with azomethines.Spectrochim Acta A Mol Biomol Spectrosc.,2010,75(1), 422-427.
  2. Janine M. Cooney, et al. Ortho-manganated arenes in synthesis: IV.Ortho-manganation of substituted acetophenones and of heteroaromatic methyl ketones. The crystal structures of two cyclometallated acetylthiophene derivatives.J. Organomet. Chem.,1988,349(1-2), 197-207.