Molecular structure of Acrolein diethyl acetal, CAS Number: 3054-95-3
Acrolein diethyl acetal (CAS 3054-95-3)
Alternate Names:
3,3-Diethoxy-1-propene
Application:
Acrolein diethyl acetal is a reagent used for the synthesis of a variety of compounds
CAS Number:
3054-95-3
Purity:
≥95%
Molecular Weight:
130.18
Molecular Formula:
C7H14O2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Acrolein diethyl acetal is a reagent used for the synthesis of a variety of compounds, including cinnamaldehydes.
Acrolein diethyl acetal (CAS 3054-95-3) References
- On the behavior of alpha,beta-unsaturated thioaldehydes and thioketones in the Diels-Alder reaction. | Li, GM., et al. 2000. J Org Chem. 65: 6601-12. PMID: 11052108
- An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides. | Battistuzzi, G., et al. 2003. Org Lett. 5: 777-80. PMID: 12605513
- Nickel-catalyzed arylation of acrolein diethyl acetal: a substitute to the 1,4-addition of arylhalides to acrolein. | Condon, S., et al. 2003. Org Lett. 5: 4701-3. PMID: 14627419
- Radical cascades using enantioenriched 7-azabenzonorbornenes and their applications in synthesis. | Hodgson, DM. and Winning, LH. 2008. Beilstein J Org Chem. 4: 38. PMID: 19043626
- Recent applications of polymer supported organometallic catalysts in organic synthesis. | Kann, N. 2010. Molecules. 15: 6306-31. PMID: 20877224
- Dehydrogenative alkenylation of uracils via palladium-catalyzed regioselective C-H activation. | Yu, YY. and Georg, GI. 2013. Chem Commun (Camb). 49: 3694-6. PMID: 23529083
- Enantioselective synthesis of spliceostatin E and evaluation of biological activity. | Ghosh, AK., et al. 2014. Org Lett. 16: 6200-3. PMID: 25423085
- Detection of Volatile Metabolites of Garlic in Human Breast Milk. | Scheffler, L., et al. 2016. Metabolites. 6: PMID: 27275838
- Recent Advances in Metal-Free Quinoline Synthesis. | Ramann, GA. and Cowen, BJ. 2016. Molecules. 21: PMID: 27483222
- Transition-State Analogues of Phenylethanolamine N-Methyltransferase. | Mahmoodi, N., et al. 2020. J Am Chem Soc. 142: 14222-14233. PMID: 32702980
- The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine. | Wang, Q., et al. 2022. Pharmaceuticals (Basel). 15: PMID: 36015147
- A triple farnesoid X receptor and peroxisome proliferator-activated receptor α/δ activator reverses hepatic fibrosis in diet-induced NASH in mice. | Heitel, P., et al. 2020. Commun Chem. 3: 174. PMID: 36703463
- Improved Process for the Synthesis of 3-(3-Trifluoromethylphenyl)propanal for More Sustainable Production of Cinacalcet HCl. | Rathod, VD., et al. 2023. Molecules. 28: PMID: 37630295
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Acrolein diethyl acetal, 25 g | sc-239197 | 25 g | $67.00 |