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[ CAS No. 37552-81-1 ] {[proInfo.proName]}

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Chemical Structure| 37552-81-1
Chemical Structure| 37552-81-1
Structure of 37552-81-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 37552-81-1 ]

CAS No. :37552-81-1 MDL No. :MFCD04972771
Formula : C5H2ClF3N2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 182.53 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 37552-81-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 32.04
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 2.08
Log Po/w (WLOGP) : 3.3
Log Po/w (MLOGP) : 1.33
Log Po/w (SILICOS-IT) : 2.61
Consensus Log Po/w : 2.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.62
Solubility : 0.438 mg/ml ; 0.0024 mol/l
Class : Soluble
Log S (Ali) : -2.25
Solubility : 1.02 mg/ml ; 0.00561 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.15
Solubility : 0.128 mg/ml ; 0.0007 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 37552-81-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362+P364-P403+P233-P501 UN#:N/A
Hazard Statements:H227-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 37552-81-1 ]

* 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 [ 37552-81-1 ]

[ 37552-81-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-85-0 ]
  • [ 37552-81-1 ]
  • [ 845616-55-9 ]
YieldReaction ConditionsOperation in experiment
56.6% With triethylamine; In DMF (N,N-dimethyl-formamide); at 100.0℃; for 5.0h; A solution of 4-chloro-6-(trifluoromethyl)pyrimidine (1.0 g, 5.48 mmol), piperazine (2.36 g, 27.4 mmol), and triethylamine (2.29 mL, 16.4 mmol) in DMF (20 mL) was stirred at 100 C. for 5 h. The reaction solution was diluted with water and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography (10% MeOH/5% Et3N/EtOAc) to yield the desired product (720 mg, 56.6%). LCMS calculated for C9H12F3N4: (M+1) 233.1; found 233.1.
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