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[ CAS No. 121643-44-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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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| 121643-44-5
Chemical Structure| 121643-44-5
Structure of 121643-44-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 121643-44-5 ]

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Product Details of [ 121643-44-5 ]

CAS No. :121643-44-5 MDL No. :MFCD00153202
Formula : C7H6F3NO Boiling Point : -
Linear Structure Formula :- InChI Key :SSAZZVQVJJXPMB-UHFFFAOYSA-N
M.W : 177.12 Pubchem ID :2775309
Synonyms :

Calculated chemistry of [ 121643-44-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 35.73
TPSA : 22.12 ?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) : -5.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.99
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 3.26
Log Po/w (MLOGP) : 1.65
Log Po/w (SILICOS-IT) : 2.34
Consensus Log Po/w : 2.26

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.46
Solubility : 0.612 mg/ml ; 0.00346 mol/l
Class : Soluble
Log S (Ali) : -2.13
Solubility : 1.31 mg/ml ; 0.00737 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.04
Solubility : 0.163 mg/ml ; 0.00092 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.8

Safety of [ 121643-44-5 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P233-P240-P241+P242+P243-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P403+P235-P501 UN#:1993
Hazard Statements:H225-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 121643-44-5 ]

* 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 [ 121643-44-5 ]

[ 121643-44-5 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 67-56-1 ]
  • [ 65753-47-1 ]
  • [ 121643-44-5 ]
  • 2
  • [ 67-56-1 ]
  • [ 124-41-4 ]
  • [ 65753-47-1 ]
  • [ 121643-44-5 ]
YieldReaction ConditionsOperation in experiment
for 18h;Heating / reflux; EXAMPLE 2Synthesis of Additional Representative Substituted Biaryl Ouinolin-4-ylamine AnaloguesA. 5-Trifluoromethyl-6-[8-('5-trifluoromethyl-pyridm-2-ylammo)-pyrido[2,3-&lpyrazin-3-yll- nicotinamide (compound 4) 1. 2-Methoxy-3-trifluoromethyl-pyridine Heat a mixture of 2-chloro-3-trifluoromethyl-pyridine (1.8 g, 10 mmol) and sodium methoxide (4M, 5 mL, 20 mmol) in MeOH (20 mL) at reflux for 18 hours. Cool the mixture and remove the volatiles by rotary evaporation. Dissolve the residue in EtOAc (50 mL) and wash with water (50 mL), saturated NaHCO3(aq) (50 mL) and brine (50 mL). Dry the organic extract overMgSO4 and remove the solvent under reduced pressure to yield the title compound.
  • 3
  • [ 121643-44-5 ]
  • 3-trifluoromethyl-pyridin-2-ol hydrobromide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With water; hydrogen bromide; acetic acid; for 1h;Heating / reflux; 2. 3-Trifluoromethyl-pyridin-2-ol EPO <DP n="53"/>Heat a mixture of <strong>[121643-44-5]2-methoxy-3-trifluoromethyl-pyridine</strong> (1.0 g, 5.6 mmol) and 30% HBr in acetic acid (5 mL) at reflux for 1 hour. Cool the mixture and remove the volatiles by rotary evaporation. Add ether and collect the precipitate by filtration. Air-dry to give the title compound as the hydrogen bromide salt.
  • 4
  • [ 121643-44-5 ]
  • [ 140-88-5 ]
  • [ 1291078-61-9 ]
  • 5
  • [ 121643-44-5 ]
  • [ 1354691-89-6 ]
  • 6
  • [ 121643-44-5 ]
  • 4-(azetidin-3-yloxy)-(6-(6-methoxy-5-trifluoromethyl-pyridin-3-yl)-5, 6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine) ditrifluoroacetate [ No CAS ]
  • 7
  • [ 121643-44-5 ]
  • {3-[6-(6-methoxy-5-trifluoromethyl-pyridin-3-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yloxy]-azetidin-1-yl}-(tetrahydro-pyran-4-yl)-methanone [ No CAS ]
  • 10
  • [ 121643-44-5 ]
  • [ 1354692-00-4 ]
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