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[ CAS No. 2160-89-6 ] {[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+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
3d Animation Molecule Structure of 2160-89-6
Chemical Structure| 2160-89-6
Chemical Structure| 2160-89-6
Structure of 2160-89-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 2160-89-6 ]

CAS No. :2160-89-6 MDL No. :MFCD00040104
Formula : C6H4F6O2 Boiling Point : -
Linear Structure Formula :- InChI Key :MNSWITGNWZSAMC-UHFFFAOYSA-N
M.W :222.09 Pubchem ID :75096
Synonyms :

Safety of [ 2160-89-6 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P261-P273-P305+P351+P338 UN#:3272
Hazard Statements:H225-H315-H319-H335-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2160-89-6 ]

* 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 [ 2160-89-6 ]

[ 2160-89-6 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 2160-89-6 ]
  • [ 73365-02-3 ]
  • [ 916823-47-7 ]
  • C23H36N2O7 [ No CAS ]
  • 2
  • [ 2160-89-6 ]
  • [ 95715-87-0 ]
  • (R)-tert-butyl 4-((S)-2-((1,1,1,3,3,3-hexafluoropropan-2-yloxy)carbonyl)-1-hydroxyallyl)-2,2-dimethyloxazolidine-3-carboxylate [ No CAS ]
  • [ 916823-59-1 ]
YieldReaction ConditionsOperation in experiment
1: 67% 2: 9% With 4-(3-ethyl-4-oxa-1-azatricyclo[4,4,0,0(3,8)]dec-5-yl)quinolin-6-ol In N,N-dimethyl-formamide at -55℃; for 73h;
  • 3
  • [ 2160-89-6 ]
  • [ 106391-88-2 ]
  • 2,6-bis((R)-1-((tert-butoxycarbonyl)amino)-2-methylpropyl)-5-methylidene-1,3-dioxan-4-one [ No CAS ]
  • tert-butyl (3S,4R)-[5-((1,1,1,3,3,3-hexafluoropropan-2-yloxy)carbonyl)-4-hydroxy-2-methylhex-5-en-3-yl]carbamate [ No CAS ]
  • tert-butyl [5-((1,1,1,3,3,3-hexafluoropropan-2-yloxy)carbonyl)-4-hydroxy-2-methylhex-5-en-3-yl]carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
18% With 4-(3-ethyl-4-oxa-1-azatricyclo[4,4,0,0(3,8)]dec-5-yl)quinolin-6-ol In N,N-dimethyl-formamide at -55℃; for 96h;
  • 4
  • [ 2160-89-6 ]
  • [ 111-27-3 ]
  • [ 104-61-0 ]
YieldReaction ConditionsOperation in experiment
82% With quinuclidin-3-yl benzenesulfonate; 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'(3H,3'H)-spirobi<2,1-benzoxasilole>; C36H16F16IrN4(1+)*F6P(1-) In acetonitrile at 20℃; for 14h; Glovebox; Inert atmosphere; Sealed tube; Irradiation;
  • 5
  • [ 2160-89-6 ]
  • [ 13379-98-1 ]
  • [ 1138501-95-7 ]
YieldReaction ConditionsOperation in experiment
75% With quinuclidin-3-yl benzenesulfonate; 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'(3H,3'H)-spirobi<2,1-benzoxasilole>; C36H16F16IrN4(1+)*F6P(1-) In acetonitrile at 20℃; for 14h; Glovebox; Inert atmosphere; Sealed tube; Irradiation;
  • 6
  • [ 15980-15-1 ]
  • [ 2160-89-6 ]
  • C10H12F6O3S [ No CAS ]
YieldReaction ConditionsOperation in experiment
91% With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate; sodium 2,2,2-trifluoroacetate In methanol; dichloromethane at 30℃; Irradiation;
  • 7
  • [ 825644-26-6 ]
  • [ 2160-89-6 ]
  • C13H8BF7O4 [ No CAS ]
  • C13H8BF7O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
90 % ee With aluminum oxide; C22H22Cl3N3O4 In 1,4-dioxane at 0℃; for 76h; enantioselective reaction;
90 % ee With aluminum oxide; C22H22Cl3N3O4 In 1,4-dioxane at 20℃; for 46h; enantioselective reaction;
  • 8
  • [ 2160-89-6 ]
  • [ 40138-17-8 ]
  • C14H11BF6O4 [ No CAS ]
  • C14H11BF6O4 [ No CAS ]
  • 9
  • [ 2160-89-6 ]
  • [ 40138-18-9 ]
  • C14H11BF6O5 [ No CAS ]
  • C14H11BF6O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
84 % ee With aluminum oxide; C22H22Cl3N3O4 In 1,4-dioxane at 20℃; for 17h; enantioselective reaction;
  • 10
  • [ 1005346-96-2 ]
  • [ 2160-89-6 ]
  • C15H13BF6O6 [ No CAS ]
  • C15H13BF6O6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
82 % ee With aluminum oxide; C22H22Cl3N3O4 In 1,4-dioxane at 20℃; for 48h; enantioselective reaction;
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