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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 3506-36-3 Chemical Structure| 3506-36-3

Structure of 3506-36-3

Chemical Structure| 3506-36-3

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Product Details of [ 3506-36-3 ]

CAS No. :3506-36-3
Formula : C11H15NO
M.W : 177.24
SMILES Code : O=C(C1=CC=CC=C1)CCN(C)C
MDL No. :MFCD00100910

Safety of [ 3506-36-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H331-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P332+P313-P362-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 3506-36-3 ]

* 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 [ 3506-36-3 ]

[ 3506-36-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 6971-44-4 ]
  • [ 3506-36-3 ]
  • 3-(Methyl-pyridin-4-ylmethyl-amino)-1-phenyl-propan-1-one [ No CAS ]
  • 2
  • [ 1455-20-5 ]
  • [ 3506-36-3 ]
  • [ 1440662-44-1 ]
YieldReaction ConditionsOperation in experiment
75% With palladium diacetate; silver carbonate; silver(l) oxide; In dimethyl sulfoxide; at 120℃; for 24h; General procedure: Synthesis of 3a-v A mixture of 1 (0.2 mmol), 2 (0.6 mmol), DMSO (3 mL),Pd(OAc)2 (5 mol%), and Ag2CO3 and Ag2O (1.5 equiv, 1:1) was stirred at 120 C under air atmosphere for 24 h. To the reaction mixture was added H2O and EtOAc, and the aqueous phase was extracted with EtOAc (3×). The combined organic layer was washed with brine, dried over Na2SO4, and evaporated under reduced pressure. The crude product was purified by silica gel column chromatography to give the corresponding products(3a,12 3g,13 3h,14 3i-l,9 3m,16 3n,17 3p,q,s-v9 according to the literature).
  • 3
  • [ 5216-17-1 ]
  • [ 3506-36-3 ]
  • [ 1440664-39-0 ]
YieldReaction ConditionsOperation in experiment
77% With palladium diacetate; silver carbonate; silver(l) oxide; In dimethyl sulfoxide; at 120℃; for 24h; General procedure: Synthesis of 3a-v A mixture of 1 (0.2 mmol), 2 (0.6 mmol), DMSO (3 mL),Pd(OAc)2 (5 mol%), and Ag2CO3 and Ag2O (1.5 equiv, 1:1) was stirred at 120 C under air atmosphere for 24 h. To the reaction mixture was added H2O and EtOAc, and the aqueous phase was extracted with EtOAc (3×). The combined organic layer was washed with brine, dried over Na2SO4, and evaporated under reduced pressure. The crude product was purified by silica gel column chromatography to give the corresponding products(3a,12 3g,13 3h,14 3i-l,9 3m,16 3n,17 3p,q,s-v9 according to the literature).
 

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