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[ CAS No. 1391728-13-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 1391728-13-4
Chemical Structure| 1391728-13-4
Structure of 1391728-13-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1391728-13-4 ]

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Product Details of [ 1391728-13-4 ]

CAS No. :1391728-13-4 MDL No. :MFCD28397076
Formula : C9H10FIO Boiling Point : No data available
Linear Structure Formula :- InChI Key :FISITPXJYDTLHI-UHFFFAOYSA-N
M.W : 280.08 Pubchem ID :72546672
Synonyms :

Safety of [ 1391728-13-4 ]

Signal Word:Danger Class:5.1
Precautionary Statements:P210-P220-P221-P280-P370+P378-P501 UN#:1479
Hazard Statements:H272 Packing Group:Ⅱ
GHS Pictogram:

Application In Synthesis of [ 1391728-13-4 ]

* 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 [ 1391728-13-4 ]

[ 1391728-13-4 ] Synthesis Path-Downstream   1~15

  • 1
  • [ 610-97-9 ]
  • [ 1391728-13-4 ]
  • 2
  • [ 69352-05-2 ]
  • [ 1391728-13-4 ]
YieldReaction ConditionsOperation in experiment
89% With silver(II) fluoride; In acetonitrile; at 20℃; for 1h;Inert atmosphere; General procedure: Under Ar atmosphere, corresponding aryl-iodides (1.0 mmol, 1.0 equiv) and AgF2 (3.3 equiv for 1; 2.5 equiv for 2) and 10 mL anhydrous MeCN were added to a 25mL rounded bottom, then the reaction mixture was allowed to stir at room temperature for 1 hour. The mixture was concentrated under vacuum. Then 20 mL anhydrous ether was added to make desired products dissolve. The mixture was filtered, and the filter cake was washed with a small amount of ether. The combined filtrate was concentrated to afford the desired product 1a-g and 2a-g in 75-95% yield
  • 3
  • [ 69352-04-1 ]
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  • 4
  • [ 1391728-13-4 ]
  • [ 887144-97-0 ]
  • 5
  • [ 134-20-3 ]
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  • 6
  • [ 69352-03-0 ]
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  • 7
  • [ 69429-70-5 ]
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  • 8
  • [ 1459128-72-3 ]
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  • 9
  • [ 1459128-73-4 ]
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  • 10
  • [ 2712-78-9 ]
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  • 11
  • [ 73602-61-6 ]
  • [ 69429-70-5 ]
  • [ 1391728-13-4 ]
  • 12
  • [ 1459128-72-3 ]
  • [ 73602-61-6 ]
  • [ 1391728-13-4 ]
  • 13
  • [ 1459128-73-4 ]
  • [ 73602-61-6 ]
  • [ 1391728-13-4 ]
  • 14
  • [ 1391728-13-4 ]
  • [ 94-02-0 ]
  • C20H21IO4 [ No CAS ]
  • 15
  • [ 1000293-91-3 ]
  • [ 1391728-13-4 ]
  • 3,3-dimethyl-1-(1,1,2,2-tetrafluoro-2-(phenylthio)ethyl)-1,3-dihydro-1λ3-benzo[d][1,2]iodaoxole [ No CAS ]
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