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[ CAS No. 128273-52-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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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+
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Chemical Structure| 128273-52-9
Chemical Structure| 128273-52-9
Structure of 128273-52-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 128273-52-9 ]

CAS No. :128273-52-9 MDL No. :MFCD06740508
Formula : C9H6F3NOS Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 233.21 Pubchem ID :-
Synonyms :

Safety of [ 128273-52-9 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501 UN#:1760
Hazard Statements:H302-H312-H314-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 128273-52-9 ]

* 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 [ 128273-52-9 ]

[ 128273-52-9 ] Synthesis Path-Downstream   1~6

YieldReaction ConditionsOperation in experiment
R.3.3 (2) (3) 1-(4-trifluoromethoxybenzyl)-3-(2,2,2-trifluoroethyl)thiourea. 6.0 g 4-trifluoromethoxybenzyl isothiocyanate obtained in (2) above and 3.06 g of 2,2,2-trifluoroethylamine were dissolved in 50 ml of ethyl acetate, and the solution was left to stand at room temperature for 24 hours. Ethyl acetate was evaporated under reduced pressure, and the resulting white crystals were recrystallized from hexane to give 6.05 g of the captioned compound. Melting point: 94.7-96.4° C. IR νneatmax (cm-1) 3240, 3060, 1570, 1510, 1300, 1250, 1180, 1170, 1150, 1110, 975, 920, 825, d1 H NMR δCDCl3 /TMS (ppm): 4.31(2H, d, J=9Hz), 4.66 (2H, s), 6.30(lH, m), 6.74(lH, m), 7.12-7.55 (9H, m).
  • 3
  • 2-(2,2,2-trifluoroethylimino)-3-(4-trifluoromethoxybenzyl)-5-phenyl-tetrahydro-1,3,5-thiadiazin-4-one [ No CAS ]
  • [ 753-90-2 ]
  • [ 128273-52-9 ]
  • [ 128273-53-0 ]
YieldReaction ConditionsOperation in experiment
In ethyl acetate R.1.3 (3) (3) 1-(4-trifluoromethoxybenzyl)-3-(2,2,2-trifluoroethyl)thiourea 6.0 g of 4-trifluoromethoxybenzyl isothiocyanate obtained in (2) above and 3.06 g of 2,2,2-trifluoroethylamine were dissolved in 50 ml of ethyl acetate, and the solution was left to stand at room temperature for 24 hours. Ethyl acetate was evaporated under reduced pressure, and the resulting white crystals were recrystallized from hexane to give 6.05 g of the captioned compound. Melting point: 94.7-96.4 oC. IR ν t(cmmin1): 3240, 3060, 1570, 1510, 1300, 1250, 1180, 1170, 1150, 1110, 975, 920, 825, 680. 1H NMR δ l3(ppm): 4.31(2H, d, J=9Hz), 4.66 (2H, s), 6.30(1H, m), 6.74(1H, m), 7.12-7.55 (9H, m).
  • 4
  • [ 463-71-8 ]
  • [ 93919-56-3 ]
  • [ 128273-52-9 ]
YieldReaction ConditionsOperation in experiment
62% Stage #1: 4-(trifluoromethoxy)benzyl amine With triethylamine In tetrahydrofuran at 0℃; for 0.166667h; Stage #2: thiophosgene In tetrahydrofuran at 0 - 20℃; for 3.33333h;
  • 5
  • [ 128273-52-9 ]
  • [ 167280-87-7 ]
  • 2-thioxo-3-(4-(trifluoromethoxy)benzyl)-2,3,6,7-tetrahydrothieno[3,2-d]pyrimidin-4(1H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
27% With pyridine at 110℃; for 24h; Inert atmosphere;
  • 6
  • [ 128273-52-9 ]
  • [ 167280-87-7 ]
  • 2-((4-oxo-3-(4-(trifluoromethoxy)benzyl)-3,4,6,7-tetrahydrothieno[3,2-d]pyrimidin-2-yl)thio)-N-(6-(trifluoromethyl)benzo[d]thiazol-2-yl)acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: pyridine / 24 h / 110 °C / Inert atmosphere 2: triethylamine / N,N-dimethyl-formamide / 2 h / 80 °C / Inert atmosphere
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