1-Azidoadamantane

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Names

[ CAS No. ]:
24886-73-5

[ Name ]:
1-Azidoadamantane

[Synonym ]:
adamantane-1-ylazide
MFCD00074793
1-adamantyl azide
Tricyclo[3.3.1.13,7]decane,1-azido
1-azido-adamamantane

Chemical & Physical Properties

[ Melting Point ]:
80-82ºC(lit.)

[ Molecular Formula ]:
C10H15N3

[ Molecular Weight ]:
177.24600

[ Flash Point ]:
85 °C(闭杯)

[ Exact Mass ]:
177.12700

[ PSA ]:
49.75000

[ LogP ]:
2.71826

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H228

[ Precautionary Statements ]:
P210

[ Personal Protective Equipment ]:
Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
F: Flammable;

[ Risk Phrases ]:
11

[ Safety Phrases ]:
16-33

[ RIDADR ]:
UN 1325

[ Packaging Group ]:
III

[ Hazard Class ]:
4.1

[ HS Code ]:
2929909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Adamantane
  • Adamantan-1-ol
  • 1-Fluoroadamantane
  • Tricyclo[3.3.1.13,7]decane,1-iodo-
  • Adamantan-1-amine
  • 1-Bromoadamantane
  • 2H-Pyran, tetrahydro-2-(tricyclo[3.3.1.13,7]dec-1-yloxy)
  • 3-(adamantane-1-carboxy)-4-methylthiazole-2(3H)-thione
  • N-(1-adamantoyloxy)pyridine-2-thione

DownStream

  • N-benzyladamantan-1-amine
  • N-benzylidene-1-aminoadamantane
  • Adamantan-1-amine
  • Bibenzyl
  • 1-Adamantyl isocyanate
  • Adamantan-1-ol
  • 1-Phenyladamantane
  • 3-phenyl-4-azatricyclo[4.3.1.13,8]undecane
  • 1-Adamantanamine hydrochloride
  • N-(1-adamantyl)benzamide

Customs

[ HS Code ]: 2929909090

[ Summary ]:
2929909090 other compounds with other nitrogen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Regioselective Sequential Modification of Chitosan via Azide-Alkyne Click Reaction: Synthesis, Characterization, and Antimicrobial Activity of Chitosan Derivatives and Nanoparticles.

PLoS ONE 10 , e0123084, (2015)

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 w...

Aldrichimica Acta 18 , 82, (1985)


More Articles

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