1-(azidomethyl)-2-methylbenzene(SALTDATA: FREE)

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Names

[ CAS No. ]:
126799-83-5

[ Name ]:
1-(azidomethyl)-2-methylbenzene(SALTDATA: FREE)

[Synonym ]:
Peroxide,bis(2-methylbenzoyl)
o-methylbenzyl azide
Bis(o-toluoyl) peroxide
bis(2-methylbenzoyl) peroxide
2-methylbenzoic peroxyanhydride
Bis(o-methylbenzoyl) peroxide
2-methylbenzoyl peroxide
di-o-toluoyl peroxide
2-methylbenzyl azide

Chemical & Physical Properties

[ Density]:
0.772 克/cm3 在 20 °C

[ Molecular Formula ]:
C8H9N3

[ Molecular Weight ]:
147.17700

[ Flash Point ]:
-30 °C

[ Exact Mass ]:
147.08000

[ PSA ]:
49.75000

[ LogP ]:
2.25806

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H315

[ Precautionary Statements ]:
P210

[ RIDADR ]:
UN 2398 3 / PGII

[ HS Code ]:
2929909090

Precursor & DownStream

Precursor

  • α-Bromo-o-xylene
  • 2-methylbenzyl chloride
  • o-xylene
  • 2-Methylbenzyl Alcohol

DownStream

  • o-Xylylamine
  • Benzenamine,N,2-dimethyl-
  • ACETAMIDE, N-[(2-METHYLPHENYL)METHYL]-
  • 2-methyl-benzenemethanaminhydrochloride
  • Triphenylphosphine oxide

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

A copper(I) isonitrile complex as a heterogeneous catalyst for azide-alkyne cycloaddition in water.

Org. Lett. 13 , 1102-1105, (2011)

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. Nota...

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...


More Articles


Related Compounds

  • 1-(azidomethyl)-4-methylbenzene(SALTDATA: FREE)
  • 1-(azidomethyl)-4-fluorobenzene(SALTDATA: FREE)
  • 1-(2-bromobutanoyl)azepane(SALTDATA: FREE)
  • 1-(Azidomethyl)-2-fluorobenzene solution
  • 1-(azidomethyl)-2-bromobenzene
  • 1-(azidomethyl)-2-nitrobenzene
  • 5-(3-{[(Tert-butoxy)carbonyl]amino}propoxy)pentanoic acid
  • 3-(6-Chloropyridin-2-yl)butan-1-amine
  • 1-(5-Amino-2-bromo-phenyl)hexahydropyrimidine-2,4-dione
  • 5-[4-[(5,6-dimethylpyrimidin-4-yl)amino]piperidin-1-yl]-1,3-dimethyl-5H-pyrimidin-1-ium-2,4-dione
  • 3-Benzyl-1-(cyclobutylmethyl)-4a,5,6,7,8,8a-hexahydroquinazoline-2,4-dione
  • methyl 2-[(4-formyl-3-methyl-1H-pyrazol-1-yl)methyl]-3-methoxybenzoate
  • 3-[2-(4-amino-1H-pyrazol-1-yl)ethoxy]propanenitrile
  • 5-(2,2-Dimethylazetidin-1-yl)pyridine-2-carbaldehyde
  • Tert-butyl 3-(4,6-dichloropyridin-2-yl)piperazine-1-carboxylate
  • 1-(5,6-Dichloropyridin-3-yl)cyclopentan-1-amine
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