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[ CAS No. 27126-93-8 ] {[proInfo.proName]}

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Chemical Structure| 27126-93-8
Chemical Structure| 27126-93-8
Structure of 27126-93-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 27126-93-8 ]

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Product Details of [ 27126-93-8 ]

CAS No. :27126-93-8 MDL No. :MFCD00000379
Formula : C9H3F6N Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 239.12 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 27126-93-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 7.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.16
TPSA : 23.79 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 3.97
Log Po/w (WLOGP) : 5.9
Log Po/w (MLOGP) : 3.51
Log Po/w (SILICOS-IT) : 3.91
Consensus Log Po/w : 3.85

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 1.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.97
Solubility : 0.0257 mg/ml ; 0.000107 mol/l
Class : Soluble
Log S (Ali) : -4.17
Solubility : 0.0161 mg/ml ; 0.0000675 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.26
Solubility : 0.0131 mg/ml ; 0.0000546 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.89

Safety of [ 27126-93-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 27126-93-8 ]

* 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 [ 27126-93-8 ]

[ 27126-93-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 328-72-3 ]
  • [ 27126-93-8 ]
YieldReaction ConditionsOperation in experiment
65% Example 8 As Example 3, but 24.9 g of <strong>[328-72-3]3,5-(bistrifluoromethyl)chlorobenzene</strong> were reacted. 15.5 g of 3,5-(bistrifluoromethyl)benzonitrile were isolated as a colorless liquid (65% of theory).
In butanone; STR7 Preparation of 3,5-bis-(trifluoromethyl)-benzonitrile By the method of Example 3, 124 g of 1-chloro-3,5-bis-(trifluoromethyl)-benzene in 120 ml of ethyl methyl ketone gave 61.4 g (51.2% of theory) of 3,5-bis-(trifluoromethyl)-benzonitrile (b.p.45 mbar: 88 C.). After 20 hours, the conversion was approximately 60%. 4.5% of coupling products had formed.
  • 3
  • [ 27126-93-8 ]
  • [ 80-17-1 ]
  • [ 21221-93-2 ]
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