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[ CAS No. 2267-23-4 ] {[proInfo.proName]}

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Chemical Structure| 2267-23-4
Chemical Structure| 2267-23-4
Structure of 2267-23-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2267-23-4 ]

CAS No. :2267-23-4 MDL No. :MFCD00042326
Formula : C7H5F3N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :YCGFVAPIBALHRT-UHFFFAOYSA-N
M.W : 222.12 Pubchem ID :2775772
Synonyms :

Calculated chemistry of [ 2267-23-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 3
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.35
TPSA : 81.07 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.51
Log Po/w (XLOGP3) : 3.07
Log Po/w (WLOGP) : 3.34
Log Po/w (MLOGP) : 0.54
Log Po/w (SILICOS-IT) : -0.38
Consensus Log Po/w : 1.62

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.25
Solubility : 0.125 mg/ml ; 0.000563 mol/l
Class : Soluble
Log S (Ali) : -4.44
Solubility : 0.00808 mg/ml ; 0.0000364 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -2.05
Solubility : 1.96 mg/ml ; 0.00883 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.3

Safety of [ 2267-23-4 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P305+P351+P338-P311 UN#:2811
Hazard Statements:H302+H312-H315-H319-H331-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2267-23-4 ]

* 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.

  • Upstream synthesis route of [ 2267-23-4 ]
  • Downstream synthetic route of [ 2267-23-4 ]

[ 2267-23-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 2267-23-4 ]
  • [ 95668-21-6 ]
YieldReaction ConditionsOperation in experiment
78% With tert.-butylnitrite; copper(ll) bromide In acetonitrile at 20℃; for 1 h; INTERMEDIATE 244-Bromo-3-nitrophenyl trifiuoromethyl ether To a solution of 2-nitro-4-[(trifluoromethyl)oxy]aniline (2.0 g, 9.0 mmol) in acetonitrlle (50 mL) was added tert-butylnitrite (7.4 g, 72 mmol). The solution was stirred 2 min and then Copper(II) bromide (40 g, 180 mmol) was added. The solution stirred for 1 h at rt. The reaction was partitioned between EtOAc (500 mL) and 1N HCl (aq) (100 mL). The layers were separated, and the organics were washed with 1N HCl (aq) (3.x.50 mL), dried over MgSO4, filtered, and the volatiies were evaporated under reduced pressure, and the residue was purified by flash column chromatography (0 to 20percent EtOAc:hexanes) to give 2.0 g (78percent) of the title compound. 1H NMR (400 MHz, CDCl3): δ 7.78 (d, J=8.79 Hz, 1H), 7.76 (s, 1H), 7.32 (s, 1H, J=8.79 Hz).
78% With tert.-butylnitrite; copper(ll) bromide In acetonitrile at 20℃; for 1 h; Intermediate 24: 4-Bromo-3-πitrQphenyi..trjflMQ.romet.h.y.J..etherTo a solution of 2-nitro-4-[(tπ^uoromoethyi)oxy]arsHine (2.0 g, 9.0 mrno.) "m acetoπitrile (50 mL) was added te/.pound.butyinitrite (7.4 g, 72 mmol). The solution was stirred 2 min and then Copper(ll) bromide (40 g, 180 mmol) was added. The solution stirred for 1 h at rt The reaction was partitioned between EtOAc (500 rπL) and 1 N HCi (aq) (100 mL). The iayers were separated, and the organics were washed mth 1N HCi (aq) (3 x 50 ml), dried over .VlgS04, filtered, and the volatiles were evaporated under reduced pressure, and the residue was purified by flash column chromatography (0 to 20percent <n="117"/>EiOAc:hexanes) to give 2,0 g (78percent) of the title compound. 1H NMR (400 MHz, CDCI3): δ 7.78 (ds J- 8.79 Hz, 1H), 7,76 (s, IH), 7,32 (s, 1 H, J- 8.79 Hz).
Reference: [1] Patent: US2008/300247, 2008, A1, . Location in patent: Page/Page column 50
[2] Patent: WO2007/143456, 2007, A2, . Location in patent: Page/Page column 115-116
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