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[ CAS No. 467435-07-0 ] {[proInfo.proName]}

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Chemical Structure| 467435-07-0
Chemical Structure| 467435-07-0
Structure of 467435-07-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 467435-07-0 ]

CAS No. :467435-07-0 MDL No. :MFCD08459292
Formula : C7H3BrClF3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FJANWAMBKVZTRG-UHFFFAOYSA-N
M.W : 259.45 Pubchem ID :20269848
Synonyms :

Calculated chemistry of [ 467435-07-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.15
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.4
Log Po/w (XLOGP3) : 4.13
Log Po/w (WLOGP) : 5.27
Log Po/w (MLOGP) : 4.66
Log Po/w (SILICOS-IT) : 4.17
Consensus Log Po/w : 4.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.35
Solubility : 0.0115 mg/ml ; 0.0000442 mol/l
Class : Moderately soluble
Log S (Ali) : -3.84
Solubility : 0.0378 mg/ml ; 0.000146 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.75
Solubility : 0.00456 mg/ml ; 0.0000176 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.56

Safety of [ 467435-07-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 467435-07-0 ]

* 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 [ 467435-07-0 ]

[ 467435-07-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 445-13-6 ]
  • [ 467435-07-0 ]
YieldReaction ConditionsOperation in experiment
50% With tert.-butylnitrite; copper(ll) bromide; In acetonitrile; at 45℃; for 3h; A solution of 4-amino-2-chlorobenzotrifluoride (9.780 g; 50.007 mmol) in MeCN (65 ml) was treated with copper(ll) bromide (1 1.169 g; 50.007 mmol), and the green heterogeneous mixture was heated to 45C. A solution of tert-butyl nitrite (6.53 ml; 55.008 mmol) in MeCN (10 ml) was then added dropwise over 30 min., and the resulting mixture was further stirred at 45C for 2h20. The dark heterogeneous reaction mixture was allowed to cool to rt, and was directly purified by FC (DCM). After concentration to dryness under reduced pressure, the expected product 4-bromo-2-chloro-1-trifluoromethyl-benzene was obtained as a yellow oil (12.82O g; 50%). LC-MS: tR = 1.10 min.; [M+H]+: no ionisation.
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