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[ CAS No. 84228-44-4 ] {[proInfo.proName]}

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Chemical Structure| 84228-44-4
Chemical Structure| 84228-44-4
Structure of 84228-44-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 84228-44-4 ]

CAS No. :84228-44-4 MDL No. :MFCD01320686
Formula : C8H8ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :WKVJBYKFGNVWLM-UHFFFAOYSA-N
M.W : 185.61 Pubchem ID :1515284
Synonyms :

Calculated chemistry of [ 84228-44-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.14
TPSA : 52.32 ?2

Pharmacokinetics

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

Lipophilicity

Log Po/w (iLOGP) : 1.89
Log Po/w (XLOGP3) : 2.75
Log Po/w (WLOGP) : 1.72
Log Po/w (MLOGP) : 1.91
Log Po/w (SILICOS-IT) : 1.61
Consensus Log Po/w : 1.98

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.96
Solubility : 0.203 mg/ml ; 0.00109 mol/l
Class : Soluble
Log S (Ali) : -3.5
Solubility : 0.0582 mg/ml ; 0.000314 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.344 mg/ml ; 0.00185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 84228-44-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 84228-44-4 ]

* 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 [ 84228-44-4 ]

[ 84228-44-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 84228-44-4 ]
  • [ 214759-66-7 ]
YieldReaction ConditionsOperation in experiment
68%
Stage #1: With tert.-butylnitrite; boron trifluoride diethyl etherate In diethyl ether; dichloromethane at -20 - 20℃; for 72.5 h;
Stage #2: at 0 - 20℃; for 18.5 h;
Stage #3: With iron(III) chloride In water at 20℃; for 0.5 h;
A solution of methyl 4-amino-3-chlorobenzoate (5.0 g, 27 mmol) was stirred at -20°C in DCM (20 mL) and treated sequentially with a solution of BF3.0Et.2 (5.5 mL, 43 mmol) in anhydrous diethyl ether (10 mL) and ferf-butyl nitrite (6.0 mL, 46 mmol). The reaction mixture was stirred at -20°C for 30 min and then allowed to warm slowly to RT and stirred for 72 h. The reaction mixture was filtered and the precipitate was washed sequentially with DCM (50 mL), Et.20 (50 mL) and isohexane (50 mL) to afford the intermediate diazonium salt. The salt was dissolved in H2O (200 mL) and slowly added to a stirred mixture of potassium cyanide (1.98 g, 30.4 mmol) and copper (I) cyanide (2.73 g, (0572) 30.4 mmol) in H20 (300 mL) at 0-5°C. After the addition the mixture was stirred at 0-5°C for 0.5 h, then at RT for 18 h. The mixture was treated with 10percent aqueous FeC solution (200 mL) and stirred at RT for 30 min. The product was extracted with EtOAc (3 x 200 mL) and the combined organic extracts were washed with brine (400 mL), dried over MgSC , filtered and concentrated in vacuo. The product was purified by silica gel chromatography (120 g, 0-10percent EtOAc in isohexane) to afford the title compound (2) (3.56 g, 68percent) as an orange solid: m/z 196 [M+H]+ (ES+); 1 H NMR (400 MHz, DMSO-d6) δ: 8.17 - 8.14 (2H, m), 8.04 (1 H, dd), 3.91 (3H, s)
Reference: [1] Patent: WO2016/97004, 2016, A1, . Location in patent: Page/Page column 67; 68
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