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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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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 111759-98-9 Chemical Structure| 111759-98-9

Structure of 111759-98-9

Chemical Structure| 111759-98-9

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Product Details of [ 111759-98-9 ]

CAS No. :111759-98-9
Formula : C5H10F2N2
M.W : 136.14
SMILES Code : FC(C1NCCNC1)F
MDL No. :MFCD19219839

Safety of [ 111759-98-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H400
Precautionary Statements:P273-P280-P305+P351+P338-P310
Class:8
UN#:3263
Packing Group:

Application In Synthesis of [ 111759-98-9 ]

* 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 [ 111759-98-9 ]

[ 111759-98-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5780-66-5 ]
  • [ 111759-98-9 ]
  • 2
  • [ 5780-66-5 ]
  • [ 111759-98-9 ]
YieldReaction ConditionsOperation in experiment
With diethylamino-sulfur trifluoride; hydrogen; In methanol; dichloromethane; EXAMPLE 112 7-[3-(Difluoromethyl)-1-piperazinyl]-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid A mixture of 3.54 g of pyrazine carboxaldehyde and 5.63 g of diethylaminosulfurtrifluoride were reacted as described by W. J. Middeton, J. of Chemistry, 40, 577 (1975). The product was purified by chromatography, then hydrogenated at 20 C. under 50 psi hydrogen with 0.58 g of platinum oxide in methanol for 4 hours. The product was collected and purified by chromatography, giving 100 mg of 3-difluoromethylpiperazine.
In methanol; dichloromethane; A 3.54 g portion of 2-<strong>[5780-66-5]pyrazinecarboxaldehyde</strong> in dichloromethane was stirred at -70 C. under a water free atmosphere. To this was added 5.63 g (4.3 ml) of diethylaminosulfurtrifluoride dropwise. The solution was allowed to warm to room temperature, then stirred overnight, filtered through Florisil (exotherm) and chromatographed on a column of silica gel, eluding with ether:hexane (1:1). The solvent was evaporated and the residue hydrogenated at 20 C. under 50 psi hydrogen with 0.58 g of platinum oxide catalyst in methanol in a Parr shaker for 4 hours. The mixture was filtered through diatomaceous earth. The filtrate was chromatographed on alumina, eluding with ether, then dichloromethane:ether (1:1), then dichloromethane and finally 5% methanol in dichloromethane, giving 100 mg of the desired compound as hygroscopic crystals.
 

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