744980
1-(Azidomethyl)-2-methylbenzene solution
~0.5 M in tert-butyl methyl ether, ≥97.0% (HPLC)
Synonym(s):
α-Azido-o-xylene solution, o-Methylbenzyl azide solution
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About This Item
Empirical Formula (Hill Notation):
C8H9N3
CAS Number:
Molecular Weight:
147.18
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4860454
Assay:
≥97.0% (HPLC)
Form:
liquid
InChI
1S/C8H9N3/c1-7-4-2-3-5-8(7)6-10-11-9/h2-5H,6H2,1H3
SMILES string
Cc1ccccc1CN=[N+]=[N-]
InChI key
TWZXVFYNRLIXRY-UHFFFAOYSA-N
assay
≥97.0% (HPLC)
form
liquid
reaction suitability
reaction type: click chemistry
concentration
~0.5 M in tert-butyl methyl ether
impurities
≤2.0% water
storage temp.
2-8°C
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-18.4 °F
flash_point_c
-28 °C
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Meina Liu et al.
Organic letters, 13(5), 1102-1105 (2011-02-12)
A structurally well-defined copper(I) isonitrile complex is shown to be an efficient, heterogeneous catalyst for the Huisgen azide-alkyne 1,3-dipolar cycloaddition under mild conditions in water. Notably, this catalyst can also be utilized in a three-component reaction of halides, sodium azide
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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