3-Acetylindole (High Purity)
Original price was: $1,395.00.$695.00Current price is: $695.00.
Catalog Number: B2014690 (10 g)
3-Acetylindole (High Purity) is a high quality substituted indole and a reactant in the first step of multiple biological synthesis applications. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
Live enquiry about this product via Text/SMS: 1-858-900-3210.
In stock
Product Description
3-Acetylindole (High Purity)
Catalog number: B2014690
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 g
Molecular Weight or Concentration: 159.19
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: 2-8°C , Dark
Keywords: 3-Acetylindole
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.
References:
1: Li JF, Yin B, Wang JJ. Mechanistic Insights into Cobalt-Catalyzed Regioselective C4-Alkenylation of 3-Acetylindole: A Detailed Theoretical Study J Org Chem. 2022 Nov 4;87(21):14125-14136.
2: Głowacka IE, Balzarini J, Piotrowska DG. 1-Amino-3-(1H-1,2,3-triazol-1-yl)propylphosphonates as acyclic analogs of nucleotides Arch Pharm (Weinheim). 2014 Jul;347(7):496-505.
3: Hachuła B, Pyzik A, Nowak M, Kusz J. Low-temperature study of 3-acetylindole at 110 K Acta Crystallogr C. 2008 Jul;64(Pt 7):o398-401.
4: Banjare SK, Nanda T, Ravikumar PC. Cobalt-Catalyzed Regioselective Direct C-4 Alkenylation of 3-Acetylindole with Michael Acceptors Using a Weakly Coordinating Functional Group Org Lett. 2019 Oct 4;21(19):8138-8143.
5: Abdel-Gawad H, Mohamed HA, Dawood KM, Badria FA. Synthesis and antiviral activity of new indole-based heterocycles Chem Pharm Bull (Tokyo). 2010 Nov;58(11):1529-31.
6: Badria FA, Soliman SM, Atef S, Islam MS, Al-Majid AM, Dege N, Ghabbour HA, Ali M, El-Senduny FF, Barakat A. Anticancer Indole-Based Chalcones: A Structural and Theoretical Analysis Molecules. 2019 Oct 16;24(20):3728.
7: El-Sayed NS, Shirazi AN, El-Meligy MG, El-Ziaty AK, Nagib ZA, Parang K. Synthesis of 4-aryl-6-indolylpyridine-3-carbonitriles and evaluation of their antiproliferative activity Tetrahedron Lett. 2014 Feb 5;55(6):1154-1158.
8: Shukla VK, Al-Abdullah ES, El-Emam AA, Sachan AK, Pathak SK, Kumar A, Prasad O, Bishnoi A, Sinha L. Spectroscopic (FT-IR, FT-Raman, and UV-visible) and quantum chemical studies on molecular geometry, Frontier molecular orbitals, NBO, NLO and thermodynamic properties of 1-acetylindole Spectrochim Acta A Mol Biomol Spectrosc. 2014 Dec 10;133:626-38.
9: Chotpatiwetchkul W, Chotsaeng N, Laosinwattana C, Charoenying P. Structure-Activity Relationship Study of Xanthoxyline and Related Small Methyl Ketone Herbicides ACS Omega. 2022 Aug 11;7(33):29002-29012.
10: Abo-Salem HM, Abd El Salam HA, Abdel-Aziem AM, Abdel-Aziz MS, El-Sawy ER. Synthesis, Molecular Docking, and Biofilm Formation Inhibitory Activity of Bis(Indolyl)Pyridines Analogues of the Marine Alkaloid Nortopsentin Molecules. 2021 Jul 6;26(14):4112.
Products Related to 3-Acetylindole (High Purity) can be found at Chemicals
Additional Information
| Weight | 0.8 oz |
|---|---|
| Dimensions | 2 × 0.9 × 0.9 in |
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