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[ CAS No. 697-86-9 ] {[proInfo.proName]}

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Chemical Structure| 697-86-9
Chemical Structure| 697-86-9
Structure of 697-86-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 697-86-9 ]

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Product Details of [ 697-86-9 ]

CAS No. :697-86-9 MDL No. :MFCD00040936
Formula : C6H4BrCl2N Boiling Point : No data available
Linear Structure Formula :- InChI Key :DTPADCOGQUOGHT-UHFFFAOYSA-N
M.W : 240.91 Pubchem ID :2756901
Synonyms :

Calculated chemistry of [ 697-86-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.57
TPSA : 26.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.11 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.19
Log Po/w (XLOGP3) : 3.75
Log Po/w (WLOGP) : 3.35
Log Po/w (MLOGP) : 3.41
Log Po/w (SILICOS-IT) : 3.1
Consensus Log Po/w : 3.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.14
Solubility : 0.0174 mg/ml ; 0.0000724 mol/l
Class : Moderately soluble
Log S (Ali) : -3.99
Solubility : 0.0247 mg/ml ; 0.000103 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.13
Solubility : 0.0179 mg/ml ; 0.0000743 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.71

Safety of [ 697-86-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 697-86-9 ]

* 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 [ 697-86-9 ]

[ 697-86-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 697-86-9 ]
  • [ 81067-38-1 ]
YieldReaction ConditionsOperation in experiment
With sodium nitrite;copper(I) chloride; In hydrogenchloride; chloroform; sulfuric acid; acetic acid; 1. 2,3,5-Trichlorobromobenzene Sodium nitrite (3.88 g, 0.056 mole) was added in portions to concentrated sulphuric acid (28.16 ml) stirred below 10 C. A solution of 2-bromo-4,6-dichloroaniline (12 g, 0.05 mole, Lancaster) in glacial acetic acid (126 ml) was added maintaining the temperature below 10 C. The mixture was stirred below 10 C. for 1 hr and then slowly added to a stirred solution of cuprous chloride (10.11 g, 0.10 mole) in concentrated hydrochloric acid (101.05 ml) at room temperature. The mixture was then stirred at room temperature for 17 hrs. The product was filtered, washed with water (3*50 ml), dissolved in chloroform (150 ml), dried over anhydrous magnesium sulphate, filtered and the filtrate evaporated in vacuo to give the desired product. Yield 10 g (77%), M.p. 55-57 C.
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