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Sigma-Aldrich

N-Hydroxy-5-norbornene-2,3-dicarboxylic acid imide

97%

Synonym(s):

N-Hydroxybicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid imide, HONB

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About This Item

Empirical Formula (Hill Notation):
C9H9NO3
CAS Number:
Molecular Weight:
179.17
Beilstein:
13540
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

form

solid

mp

165-170 °C (lit.)

SMILES string

ON1C(=O)[C@@H]2[C@H]3C[C@H](C=C3)[C@@H]2C1=O

InChI

1S/C9H9NO3/c11-8-6-4-1-2-5(3-4)7(6)9(12)10(8)13/h1-2,4-7,13H,3H2/t4-,5+,6-,7+

InChI key

ZUSSTQCWRDLYJA-UMRXKNAASA-N

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Application

N-Hydroxy-5-norbornene-2,3-dicarboxylic acid imide (NHND) can be used as an internal reference for the determination of OH content by the phosphytilation method. It can also be used as a solid mediator for the oxidation reaction of fullerene.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Polymer-assisted biocatalysis: Unprecedented enzymatic oxidation of fullerene in aqueous medium
Gitsov I, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 50(1), 119-126 (2012)
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In this article, the functional group composition of the spruce (Pícea ábies) and birch (Bétula péndula) phloem lignin is described. The features of the chemical structure were studied by analyzing dioxane lignin using the elemental analysis, UV-Vis, FT-IR, and 1D
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Dual-functioning additives with plasticizing and antibacterial functions were designed by exploiting the natural aromatic compound eugenol and green platform chemical levulinic acid or valeric acid that can be produced from biobased resources. One-pot synthesis methodology was utilized to create three
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The preparation of nanoparticles represents a powerful tool for lignin valorization, as it combines easy methodologies with high application potential. Different synthetic strategies and various lignin sources have been employed in the process. However, the great variability in the lignin
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Technical lignins, typically obtained from the biorefining of lignocellulosic raw materials, represent a highly abundant natural aromatic feedstock with high potential in a sustainable economy scenario, especially considering the huge primary production volumes and the inherently renewable nature of this

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