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3-Acetylindole (High Purity) Chemicals Molecular Depot
3-Acetylindole (High Purity) Chemicals Molecular Depot
3-Acetylindole (High Purity) Chemicals Molecular Depot
3-Acetylindole (High Purity) Chemicals Molecular Depot

3-Acetylindole (High Purity)

$907.00

    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.

    Products are for in vitro research use only (RUO).

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What's Included

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VR Headset

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2 Touch Controllers

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Charging Cable

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Power Adapter

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Glasses Spacer

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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

  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.

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Product Resources:

Copy of Technical Specifications

FeatureDetails
Viewing Head Siedentopf type trinocular head, inclined at 30°, Interpupillary adjustment 53mm to 75mm, graduated diopter on left eyetube (30mm I.D. eyetubes)
Eyepieces SWH10X Widefield high eyepoint eyepiece, Field No. 22, tube O.D. 30.0 mm
Nosepiece Quintuple
Quintuple LWD Planachromat Phase 10x, 20x
Condenser TC Condenser N.A. 0.30, W.D. 73.0mm
Stage180mm(X) x 245mm(Y) plain stage with replaceable glass insert with 45mm opening, Glass Stage plate insert
IlluminationKoehler without iris, with phase slider, 3W LED
WarrantyLIMITED LIFETIME WARRANTY

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