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[ CAS No. 1116-76-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1116-76-3
Chemical Structure| 1116-76-3
Structure of 1116-76-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1116-76-3 ]

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Product Details of [ 1116-76-3 ]

CAS No. :1116-76-3 MDL No. :MFCD00009560
Formula : C24H51N Boiling Point : -
Linear Structure Formula :- InChI Key :XTAZYLNFDRKIHJ-UHFFFAOYSA-N
M.W : 353.67 Pubchem ID :14227
Synonyms :

Calculated chemistry of [ 1116-76-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 25
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 21
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 120.38
TPSA : 3.24 ?2

Pharmacokinetics

GI absorption : Low
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) : -0.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 6.46
Log Po/w (XLOGP3) : 10.52
Log Po/w (WLOGP) : 8.37
Log Po/w (MLOGP) : 6.26
Log Po/w (SILICOS-IT) : 8.57
Consensus Log Po/w : 8.04

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 3.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -7.27
Solubility : 0.0000188 mg/ml ; 0.0000000532 mol/l
Class : Poorly soluble
Log S (Ali) : -10.54
Solubility : 0.0000000103 mg/ml ; 0.0 mol/l
Class : Insoluble
Log S (SILICOS-IT) : -8.84
Solubility : 0.000000516 mg/ml ; 0.0000000015 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 2.97

Safety of [ 1116-76-3 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501 UN#:3082
Hazard Statements:H302-H317-H318-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1116-76-3 ]

* 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 [ 1116-76-3 ]

[ 1116-76-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1116-76-3 ]
  • [ 652-12-0 ]
  • [ 5292-42-2 ]
YieldReaction ConditionsOperation in experiment
92.3% In methanol; EXAMPLE 18 Into a 100 ml glass reactor equipped with a reflux condenser and a stirrer, 20 g (0.091 mol) of the tetrafluorophthalic anhydride prepared in Example 3 and 32.2 g (0.091 mol) of tri-n-octylamine were charged and 3.5 g (0.109 mol) of methanol was dropwise added thereto. Then, the mixture was reacted at 140 C. for 4 hours. After completion of the reaction, the reaction mixture was separated by distillation to obtain 17.5 g of 3,4,5,6-tetrafluorobenzoic acid methyl ester. The yield was 92.3%.
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