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[ CAS No. 1889-71-0 ] {[proInfo.proName]}

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Chemical Structure| 1889-71-0
Chemical Structure| 1889-71-0
Structure of 1889-71-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1889-71-0 ]

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Product Details of [ 1889-71-0 ]

CAS No. :1889-71-0 MDL No. :MFCD00016342
Formula : C14H11ClO Boiling Point : No data available
Linear Structure Formula :- InChI Key :DXVALSKCLLBZEB-UHFFFAOYSA-N
M.W : 230.69 Pubchem ID :233840
Synonyms :

Calculated chemistry of [ 1889-71-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.07
Num. rotatable bonds : 3
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 66.13
TPSA : 17.07 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.45
Log Po/w (XLOGP3) : 3.81
Log Po/w (WLOGP) : 3.77
Log Po/w (MLOGP) : 3.78
Log Po/w (SILICOS-IT) : 4.39
Consensus Log Po/w : 3.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.03
Solubility : 0.0216 mg/ml ; 0.0000938 mol/l
Class : Moderately soluble
Log S (Ali) : -3.86
Solubility : 0.0316 mg/ml ; 0.000137 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.89
Solubility : 0.000297 mg/ml ; 0.00000129 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.55

Safety of [ 1889-71-0 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P272-P280-P305+P351+P338-P310-P302+P352-P363-P403-P501 UN#:3077
Hazard Statements:H317-H318 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1889-71-0 ]

* 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 [ 1889-71-0 ]

[ 1889-71-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 178686-24-3 ]
  • [ 57-13-6 ]
  • [ 1889-71-0 ]
  • [ 1283117-45-2 ]
YieldReaction ConditionsOperation in experiment
7.8% With hydrogenchloride; In ethanol; water;Reflux; [00181] A mixture of l-(4-chlorophenyl)-2-phenylethanone (350 mg, 1.52mmol), 3- ethoxy-4-hydroxy-5-nitrobenzaldehyde (320 mg, 1.52mmol), and urea (272 mg, 4.53mmol) in anhydrous EtOH (15 mL) was added concentrated HCl solution (0. 5 mL), and the reaction mixture was refluxed for overnight. TLC (EtOAc:MeOH=10: l) showed that about 30% of starting materials were consumed, and the reaction mixture was concentrated. The residue was purified by column chromatography (EtOAc:MeOH=40: l) and preparative HPLC to afford the product Compound 36 as a yellow solid (55.1 mg, yield: 7.8%). 1H NMR (DMSO- 6 400 MHz): delta 10.30 (s, 1H), 8.79 (s, 1H), 7.55 (s, 1H), 7.42 (s, 1H), 7.30 (d, J = 8.4 Hz, 2H), 7.20 (d, J = 8.4 Hz, 2H), 7.18 (s, 1H), 7.00-7.10 (m, 3H), 6.82 (d, J = 7.2 Hz, 2H), 5.20 (d, J = 2.4 Hz, 1H), 4.00-4.10 (m, 2H), 1.33 (t, J = 6.8 Hz, 3H); MS (ESI): m/z 466.0 [M+l]+.
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