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[ CAS No. 700-16-3 ] {[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+
Chemical Structure| 700-16-3
Chemical Structure| 700-16-3
Structure of 700-16-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 700-16-3 ]

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Product Details of [ 700-16-3 ]

CAS No. :700-16-3 MDL No. :MFCD00006225
Formula : C5F5N Boiling Point : -
Linear Structure Formula :- InChI Key :XTGOWLIKIQLYRG-UHFFFAOYSA-N
M.W : 169.05 Pubchem ID :69690
Synonyms :

Calculated chemistry of [ 700-16-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 6.0
Num. H-bond donors : 0.0
Molar Refractivity : 24.03
TPSA : 12.89 ?2

Pharmacokinetics

GI absorption : High
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) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 2.02
Log Po/w (WLOGP) : 3.88
Log Po/w (MLOGP) : 2.65
Log Po/w (SILICOS-IT) : 3.58
Consensus Log Po/w : 2.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.56
Solubility : 0.461 mg/ml ; 0.00273 mol/l
Class : Soluble
Log S (Ali) : -1.92
Solubility : 2.04 mg/ml ; 0.0121 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.42
Solubility : 0.065 mg/ml ; 0.000385 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 700-16-3 ]

Signal Word:Danger Class:3,8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2924
Hazard Statements:H225-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 700-16-3 ]

* 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 [ 700-16-3 ]

[ 700-16-3 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 700-16-3 ]
  • [ 372-47-4 ]
  • [ 2875-18-5 ]
  • [ 71902-33-5 ]
  • 4
  • [ 700-16-3 ]
  • [ 2456-81-7 ]
  • [ 943868-08-4 ]
  • 5
  • [ 700-16-3 ]
  • [ 2875-18-5 ]
  • [ 2693-66-5 ]
  • [ 76469-41-5 ]
  • [ 71902-33-5 ]
  • 6
  • [ 700-16-3 ]
  • [ 5932-27-4 ]
  • [ 1439863-71-4 ]
  • 7
  • [ 700-16-3 ]
  • [ 3512-16-1 ]
  • [ 2875-18-5 ]
  • [ 76469-41-5 ]
  • [ 71902-33-5 ]
YieldReaction ConditionsOperation in experiment
11%Spectr.; 11%Spectr.; 8%Spectr.; 6%Spectr. With triethylsilane; [Rh(mu-H)(1,3-bis(diisopropylphosphanyl)propane)]2; In benzene-d6; at 50℃; for 48h;Inert atmosphere; General procedure: To a solution of fluoroarene (0.1?M) and HSiEt3 (0.1?M) in benzene-d6 in a PFA tube alpha,alpha,alpha-trifluorotoluene (1?2?muL) was added as internal standard. The PFA tube was closed by a Teflon plug, inserted into an NMR tube and an initial 19F{1H} NMR spectrum was recorded. Then [Rh(mu-H)(dippp)]2 (1) (0.005?M) was added and the reaction mixture was heated to 50?°C for 48?h. Hydrodefluorination of pentafluoropyridine gave 2,3,5,6-tetrafluoropyridine (11percent), 2,3,4,5-tetrafluoropyridine (11percent), 2,3,5-trifluoropyridine (8percent), 3,5-difluoropyridine (6percent) and 2-fluoropyridine (1percent) (TON?=?11). Hydrodefluorination of 2,3,5,6-tetrafluoropyridine or 2,3,5,6-tetrafluoropyridine or 2,3,5,6-tetrafluoropyri-dine gave 2,3,5-trifluoropyridine (24percent), 2,3,6-trifluoropyridine (7percent), 3,5-difluoropyridine (15percent), 2,5-difluoropyridine (2percent) and 2-fluoropyridine (8percent) (TON?=?18). Hydrodefluorination of hexafluoro-benzene or hexafluoroben-zene or hexa-fluorobenzene gave pentafluorobenzene (12percent) and 1,2,4,5-tetra-fluorobenzene or 1,2,4,5-tetrafluoro-benzene or 1,2,4,5-tetrafluoroben-zene (2percent) (TON?=?3.1). Hydrodefluorination of pentafluorobenzene gave 1,2,4,5-tetrafluorobenzene (35percent), 1,2,3,4-tetrafluorobenzene (3percent), 1,2,4-trifluorobenzene (23percent) and 1,4-difluorobenzene (4percent) (TON?=?19). Yields of organic hydrodefluorination products were determined from 19F{1H} NMR spectra by integration of product resonances versus the internal standard. Hydrodefluorination products were identified by NMR spectroscopy by comparison with literature data [23]. TON: number of hydrodefluorination steps/moles of 1.
  • 9
  • [ 700-16-3 ]
  • [ 15181-11-0 ]
  • 4-(2,4-di-tert-butyl-6-methylphenyl)-2,3,5,6-tetrafluoropyridine [ No CAS ]
  • 10
  • [ 700-16-3 ]
  • [ 120341-31-3 ]
  • [ 73672-37-4 ]
  • ethyl 2-(diethoxyphosphoryloxy)-2-(pyridin-3-yl)-2-(2,3,5,6-tetrafluoropyridin-4-yl)acetate [ No CAS ]
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