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About This Item
Empirical Formula (Hill Notation):
C14H19N3O9
Molecular Weight:
373.32
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
InChI key
NHNYHKRWHCWHAJ-DGTMBMJNSA-N
SMILES string
CC(=O)OC[C@H]1O[C@H](N=[N+]=[N-])[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
InChI
1S/C14H19N3O9/c1-6(18)22-5-10-11(23-7(2)19)12(24-8(3)20)13(25-9(4)21)14(26-10)16-17-15/h10-14H,5H2,1-4H3/t10-,11-,12+,13+,14+/m1/s1
assay
≥90% (TLC)
form
solid
mp
373.3 °C
shipped in
wet ice
storage temp.
−20°C
Application
α-D-Mannopyranosyl azide tetraacetate is used to make N-linked glycopeptides in glycobiology and in "click" chemistry.
Used to make N-linked glycopeptides in glycobiology.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Steven Lal et al.
The Journal of organic chemistry, 76(7), 2367-2373 (2011-03-10)
A careful methodological study revealed a true Click catalytic system based on commercially available [CuBr(PPh(3))(3)]. This system is active at room temperature, with 0.5 mol % [Cu] (or less), in the absence of any additive, and it does not require
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