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N-Hydroxyphthalimide (Highly Pure) Chemicals Molecular Depot
N-Hydroxyphthalimide (Highly Pure) Chemicals Molecular Depot
N-Hydroxyphthalimide (Highly Pure) Chemicals Molecular Depot
N-Hydroxyphthalimide (Highly Pure) Chemicals Molecular Depot

N-Hydroxyphthalimide (Highly Pure)

$595.00

    Catalog Number: B2015630 (1 g)

    N-Hydroxyphthalimide (Highly Pure) is a high quality For preparation of amine nucleosides for coupling into non-anionic, anti-sense oligonucleosides.1. This product has been used as a 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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N-Hydroxyphthalimide (Highly Pure)

Catalog number: B2015630
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 163.13 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: 2-Hydroxy-1H-isoindole-1,3(2H)-dione, 2-Hydroxyisoindole-1,3-dione, 2-Hydroxyphthalimide
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

  • Wang J, Yi WJ. Practical N-Hydroxyphthalimide-Mediated Oxidation of Sulfonamides to N-Sulfonylimines Molecules. 2019 Oct 19;24(20):3771.
  • Shibuya M , Orihashi T , Li Y , Yamamoto Y . N-Hydroxyphthalimide-catalyzed chemoselective intermolecular benzylic C-H amination of unprotected arylalkanols Chem Commun (Camb). 2021 Sep 11;57(70):8742-8745.
  • Guo Y, Luo Y, Mu S, Xu J, Song Q. Photoinduced Decarboxylative Phosphorothiolation of N-Hydroxyphthalimide Esters Org Lett. 2021 Sep 3;23(17):6729-6734.
  • Li ZH, Fiser B, Jiang BL, Li JW, Xu BH, Zhang SJ. N-Hydroxyphthalimide/benzoquinone-catalyzed chlorination of hydrocarbon C-H bond using N-chlorosuccinimide Org Biomol Chem. 2019 Mar 27;17(13):3403-3408.
  • Ji K, Liu F, Hailemariam Barkae T, Quan S, Zeid AM, Zhang W, Li J, Xu G. Development of lucigenin-N-hydroxyphthalimide chemiluminescence system and its application to sensitive detection of Co(2) Spectrochim Acta A Mol Biomol Spectrosc. 2022 Oct 15;279:121459.
  • Tiron A, Stan CS, Luta G, Uritu CM, Vacarean-Trandafir IC, Stanciu GD, Coroaba A, Tiron CE. Manganese-Doped N-Hydroxyphthalimide-Derived Carbon Dots-Theranostics Applications in Experimental Breast Cancer Models Pharmaceutics. 2021 Nov 22;13(11):1982.
  • Wang M, Liang G, Wang Y, Fan T, Yuan B, Liu M, Yin Y, Li L. Merging N-Hydroxyphthalimide into Metal-Organic Frameworks for Highly Efficient and Environmentally Benign Aerobic Oxidation Chemistry. 2021 Jul 2;27(37):9674-9685.
  • Zhang H, Wang T, Xu K, Zeng C. N-Hydroxyphthalimide-Mediated Electrochemical Denitrogenation of Aroylhydrazides to Generate Acyl Radicals and Their Applications in the Syntheses of Fluorenones J Org Chem. 2021 Nov 19;86(22):16171-16176.
  • Biliuta G, Baron RI, Coseri S. Pullulan Oxidation in the Presence of Hydrogen Peroxide and N-Hydroxyphthalimide Materials (Basel). 2022 Sep 2;15(17):6086.

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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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