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[ CAS No. 660431-66-3 ] {[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| 660431-66-3
Chemical Structure| 660431-66-3
Structure of 660431-66-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 660431-66-3 ]

CAS No. :660431-66-3 MDL No. :MFCD07390260
Formula : C15H11F2NO2S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 307.31 Pubchem ID :-
Synonyms :

Safety of [ 660431-66-3 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P330-P332+P313-P337+P313-P361-P403+P233-P405-P501 UN#:2811
Hazard Statements:H301-H311-H315-H319-H331-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 660431-66-3 ]

* 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 [ 660431-66-3 ]

[ 660431-66-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 660431-66-3 ]
  • [ 22398-14-7 ]
  • [ 1902955-29-6 ]
YieldReaction ConditionsOperation in experiment
45% With sodium hydride In diethyl ether; acetonitrile at 0 - 40℃; for 48h; Inert atmosphere; 3 3, AB03288 synthesis Take 12g 60% NaH, 250ml ether, nitrogen protection, ice bath cooling, T = 0-10 °C drop 250ml acetonitrile dissolved 46g (IV) and 52.33g (V), drop added Stir at 40 ° C for 48 h. After the end of the reaction, 500 ml of water was added, and the mixture was extracted three times with 100 ml of MTBE. The organic phase was combined, washed with 300 mL of brine, dried over anhydrous sodium sulfate, and filtered and evaporated to remove the solvent to obtain an oily substance, and 1.5 times by weight of 100-200 silica gel was added. Mix the sample, 4 times the weight of 200-300 silica gel column, column chromatography with n-heptane: ethyl acetate = 30:1 to 15:1 gradient elution, collect the product point, concentrate under reduced pressure, add 50ml positive Heptane, 2 ml of ethyl acetate was filtered at room temperature 15-30 ° C for 1 h to give 18 g of yellow powdery solid (yield 45%, HPLC: 99.5%)
  • 2
  • [ 660431-66-3 ]
  • [ 728034-12-6 ]
  • [ 108-91-8 ]
  • 4-(1-cyclohexyl-4-(2,4-difluorophenyl)-1H-imidazol-5-yl)-1H-pyrrolo[2,3-b]pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
15% General procedure: To a solutionof the corresponding aldehyde (1.2 eq.; unless stated otherwise) in DMF (2 inL per 0.3 mmol of aldehyde; unless stated otherwise) was added the corresponding amine (2.5 eq.; unless stated otherwise) and the resulting solution was stirred at 25 C to form the corresponding inline. Then, the corresponding isocyano(tosyl)methyl)arene reagent (1 eq.; unless stated otherwise) and K2CO3 (1.5 eq.; unless stated otherwise*) were added and the reaction mixture was stirred at 25 C (unless stated otherwise). The reaction was stopped after the time indicated for each particular reaction. The reaction progress was monitored by TLC. (0083) A saturated aqueous solution of NH4CI (10 mL per 1 mmol of aldehyde) was added to the reaction mixture, which was then extracted with EtOAc (2 x 30 mL per 1 mmol of aldehyde). The combined organic extracts were washed with H2O (2 x 25 mL per 1 mmol of aldehyde), dried over MgSCC, filtered, and the solvent was evaporated in vacuo to provide the crude product. The residue obtained after the workup was purified using column chromatography or preparative TLC (unless stated otherwise). (0084) * note: in cases when the amine was used as HC1 salt, 4 eq. of K2CO3 were used
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