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[ CAS No. 22115-41-9 ] {[proInfo.proName]}

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Chemical Structure| 22115-41-9
Chemical Structure| 22115-41-9
Structure of 22115-41-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 22115-41-9 ]

CAS No. :22115-41-9 MDL No. :MFCD00001794
Formula : C8H6BrN Boiling Point : -
Linear Structure Formula :- InChI Key :QGXNHCXKWFNKCG-UHFFFAOYSA-N
M.W : 196.04 Pubchem ID :89599
Synonyms :
Chemical Name :2-Cyanobenzyl bromide

Safety of [ 22115-41-9 ]

Signal Word:Danger Class:8
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 22115-41-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 22115-41-9 ]

[ 22115-41-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2346-00-1 ]
  • [ 22115-41-9 ]
  • 2-(4,5-dihydro-1,3-thiazol-2-yl)-1H-3-indenamino [ No CAS ]
  • 2
  • [ 6086-21-1 ]
  • [ 22115-41-9 ]
  • [ 1353721-43-3 ]
  • 3
  • [ 22115-41-9 ]
  • [ 56293-29-9 ]
  • 12-N-(2-cyanobenzyl)aloperine hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% General procedure: Take <strong>[56293-29-9]aloperine</strong> (1) 0.5 g (0,002 mol),Was added to 20 ml of acetonitrile, and 1.8 g (0.006 mol) of anhydrous potassium carbonate and substituted bromobenzyl or benzyl chloride (0.003 mol) were successively added to the reaction solution, followed by stirring at room temperature.TLC was detected until the reaction was complete. The organic phase was concentrated and evaporated to dryness. The solvent was dissolved in dichloromethane and washed successively with water and saturated brine. The methylene chloride layer was dried and the solvent was evaporated to dryness with a rotary evaporator to give the crude 12-N-benzyl <strong>[56293-29-9]aloperine</strong> derivative. The solution was dissolved in 20 ml of methylene chloride solventAnd then separated by column chromatography to give pure product of 12-N-benzyl-<strong>[56293-29-9]aloperine</strong> derivative (2). The resulting compound was dissolved in 5 ml of ether,And then with 1N HCl / Et2O adjusted PH = 6-7, filtered, 12-N-benzyl ether alkalis derivatives pure hydrochloric acid.
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