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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| 38435-51-7 Chemical Structure| 38435-51-7

Structure of 38435-51-7

Chemical Structure| 38435-51-7

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Product Details of [ 38435-51-7 ]

CAS No. :38435-51-7
Formula : C8H8ClNO2
M.W : 185.61
SMILES Code : Cl/C(C1=CC=C(OC)C=C1)=N\O
MDL No. :MFCD01924588

Safety of [ 38435-51-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H314-H331
Precautionary Statements:P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P405-P501
Class:6.1(8)
UN#:2928
Packing Group:

Application In Synthesis of [ 38435-51-7 ]

* 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 [ 38435-51-7 ]

[ 38435-51-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 10601-99-7 ]
  • [ 38435-51-7 ]
  • 3-(4-methoxyphenyl)-5-(3-cyanophenyl)-isoxazole [ No CAS ]
  • 2
  • [ 21806-61-1 ]
  • [ 38435-51-7 ]
  • (3aR,6aR)-3-(4-Methoxy-phenyl)-6,6a-dihydro-3aH-1,5-dioxa-4-thia-2-aza-pentalene 4,4-dioxide [ No CAS ]
  • 4
  • [ 78-88-6 ]
  • [ 38435-51-7 ]
  • [ 325744-41-0 ]
YieldReaction ConditionsOperation in experiment
349 mg With triethylamine; at 20.0℃; for 1.0h; General procedure: A drop of pyridine and then NCS (294 mg,2.2 mmol) with stirring were added to a suspension ofoxime 1 (2 mmol) in DCP (5 ml). Dissolution of the NCStook place, followed by precipitation of succinimide. Themixture was stirred at room temperature for 30 min, thenheated to 40 for 3-24 h (TLC control). A solution ofEt3N (455 mg, 4.5 mmol) in DCP (1 ml) was added withvigorous stirring to the mixture at room temperature.Heating of the mixture and precipitation occurred. Thereaction mixture was stirred for 1 h, DCP was distilled offunder reduced pressure, and the target compound wasisolated by flash chromatography on silica gel, eluentCH2Cl2 or CHCl3, Rf 0.6-0.8.
 

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