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[ CAS No. 811-68-7 ] {[proInfo.proName]}

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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| 811-68-7
Chemical Structure| 811-68-7
Structure of 811-68-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 811-68-7 ]

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Product Details of [ 811-68-7 ]

CAS No. :811-68-7 MDL No. :MFCD25563234
Formula : CAgF3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 208.94 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 811-68-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 13.42
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.35 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.72
Log Po/w (WLOGP) : 2.31
Log Po/w (MLOGP) : 1.11
Log Po/w (SILICOS-IT) : 2.49
Consensus Log Po/w : 1.53

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.22
Solubility : 1.26 mg/ml ; 0.00604 mol/l
Class : Soluble
Log S (Ali) : -1.34
Solubility : 9.64 mg/ml ; 0.0461 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.8
Solubility : 33.0 mg/ml ; 0.158 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.04

Safety of [ 811-68-7 ]

Signal Word:Danger Class:8
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 811-68-7 ]

* 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 [ 811-68-7 ]

[ 811-68-7 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 306935-88-6 ]
  • [ 811-68-7 ]
  • [ 1333415-81-8 ]
  • 2
  • [ 811-68-7 ]
  • [ 131818-17-2 ]
  • [ 1333415-86-3 ]
  • 3
  • [ 19591-17-4 ]
  • [ 811-68-7 ]
  • [ 347-48-8 ]
  • 4
  • [ 1007-03-0 ]
  • [ 811-68-7 ]
  • (cyclopropyl(phenyl)methyl)(trifluoromethyl)sulfane [ No CAS ]
  • 5
  • [ 19936-14-2 ]
  • [ 811-68-7 ]
  • C11H10BrF3OS [ No CAS ]
  • 6
  • [ 39604-97-2 ]
  • [ 811-68-7 ]
  • (1-(4-propoxyphenyl) vinyl)(trifluoromethyl)sulfane [ No CAS ]
  • 7
  • [ 5451-55-8 ]
  • [ 811-68-7 ]
  • (4-(tert-butyl)cyclohexyl)(trifluoromethyl)sulfane [ No CAS ]
  • C11H19F3S [ No CAS ]
  • 8
  • [ 32340-38-8 ]
  • [ 811-68-7 ]
  • (E)-3-([1,1'-biphenyl]-4-yl)-2,3-bis((trifluoromethyl)thio)acrylic acid [ No CAS ]
  • 9
  • [ 932-32-1 ]
  • [ 811-68-7 ]
  • C8H7ClFNS [ No CAS ]
  • C8H7ClFNS [ No CAS ]
  • 10
  • [ 6563-13-9 ]
  • [ 811-68-7 ]
  • 6-methoxy-2-(trifluoromethylthio)quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
54% With p-toluenesulfonylanhydride; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; at 20℃; for 4h;Schlenk technique; General procedure: A mixture of heteroaryl N-oxide (0.4mmol), AgSCF3 (166.3mg, 0.8mmol), Ts2O (195.8mg, 0.6mmol), and n-Bu4NI (295.5mg, 0.8mmol) was added in a 25mL Schlenk tube, and then THF (4.0mL) was added. The mixture was stirred at room temperature for 4h. After the reaction was complete, saturated NH4Cl solution was added. The resulting mixture was extracted with EtOAc for three times. The combined organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (PE/EA=100:1) to give the desired product (2a-2w).f
  • 11
  • [ 811-68-7 ]
  • [ 127903-20-2 ]
  • C22H24FNO3S [ No CAS ]
  • 12
  • [ 811-68-7 ]
  • [ 73852-88-7 ]
  • [ 1005206-25-6 ]
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