276219
1-Azidoadamantane
97%
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About This Item
Empirical Formula (Hill Notation):
C10H15N3
CAS Number:
Molecular Weight:
177.25
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
MDL number:
Product Name
1-Azidoadamantane, 97%
InChI
1S/C10H15N3/c11-13-12-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2/t7-,8+,9-,10-
SMILES string
[N-]=[N+]=NC12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI key
JOMZSYXWYOVFEE-CHIWXEEVSA-N
assay
97%
form
powder or crystals
technique(s)
titration: suitable
mp
80-82 °C (lit.)
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
2-8°C
Quality Level
Related Categories
Application
Building block for "Anti-Bredt"strained molecules.
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Krzysztof Matyjaszewski et al.
Molecules (Basel, Switzerland), 26(2) (2021-01-14)
N-alkyl phosphoranimines were synthesized via the Staudinger reaction of four different alkyl azides with tris(2,2,2-trifluoroethyl) phosphite. N-adamantyl, N-benzyl, N-t-butyl, and N-trityl phosphoranimines were thoroughly characterized and evaluated as chain-capping compounds in the anionic polymerization of P-tris(2,2,2-trifluoroethoxy)-N-trimethylsilyl phosphoranimine monomer. All four
Aldrichimica Acta, 18, 82-82 (1985)
Atif Sarwar et al.
PloS one, 10(4), e0123084-e0123084 (2015-05-01)
Recently, the attention of researchers has been drawn toward the synthesis of chitosan derivatives and their nanoparticles with enhanced antimicrobial activities. In this study, chitosan derivatives with different azides and alkyne groups were synthesized using click chemistry, and these were
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