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-(Bromomethyl)furan-3-carbonitrile
  • 1-(4-Chlorophenyl)-1,4-dihydro-5-methoxy-4-oxo-3-cinnolinecarboxylic acid
  • 6-(1-phenylethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
  • 3-[(2R)-2-aminopropyl]-1H-indol-5-ol
  • Piperazine,1-[2-(4-chlorophenyl)-3-methyl-1-oxobutyl]-4-[4-(2-furanyl)-2-pyrimidinyl]-
  • N-{[(2-methyl-4-phenyl-1,3-thiazol-5-yl)amino]carbonyl}-1-benzothiophene-2-sulfonamide
  • N-(4-tert-butylcyclohexyl)benzylamine
  • 6-[2-(4-Sulfamoyl-phenyl)-ethylcarbamoyl]-pyridine-2-carboxylic acid
  • 4-chloro-2-cyclopropyl-5H,6H,7H,8H,9H-pyrimido[4,5-b]azepine
  • 1-Benzyl-4-[N-ethyl-N-(3-(2-methyl-1-propenyl)-2-pyridinyl)amino]piperidine
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