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[ CAS No. 791626-59-0 ] {[proInfo.proName]}

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Chemical Structure| 791626-59-0
Chemical Structure| 791626-59-0
Structure of 791626-59-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 791626-59-0 ]

CAS No. :791626-59-0 MDL No. :MFCD08236769
Formula : C10H6ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :JRXFGSDIVFFZTM-UHFFFAOYSA-N
M.W : 191.61 Pubchem ID :11252504
Synonyms :

Calculated chemistry of [ 791626-59-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 52.14
TPSA : 29.96 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 2.17
Log Po/w (WLOGP) : 2.7
Log Po/w (MLOGP) : 1.7
Log Po/w (SILICOS-IT) : 3.22
Consensus Log Po/w : 2.32

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.9
Solubility : 0.242 mg/ml ; 0.00126 mol/l
Class : Soluble
Log S (Ali) : -2.43
Solubility : 0.708 mg/ml ; 0.0037 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.27
Solubility : 0.0103 mg/ml ; 0.000054 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.27

Safety of [ 791626-59-0 ]

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

Application In Synthesis of [ 791626-59-0 ]

* 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 [ 791626-59-0 ]

[ 791626-59-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56921-01-8 ]
  • [ 791626-59-0 ]
  • [ 1001608-57-6 ]
YieldReaction ConditionsOperation in experiment
82% pyrrolidine; In methanol;Heating / reflux; A solution of compound 7.3 (1.71 g, 8.51 mmol, 1 equiv) in MeOH (35 rnL) was treated with compound 7.6 (1.63 g, 8.51 mmol, 1 equiv). The reaction mixture was heated to reflux until a solution was obtained. Then a catalytic amount of pyrrolidine (70μL,0.0605 g, 0.851 mmol, 0.10 equiv) was added. The reaction mixture was heated to reflux over-night. After cooling to RT, evaporation of the solvent gave a residue that was purified by ISCO (gradient Hex:EtOAc = 100:0 to 0:100) to afford 5-[(E)-2-(2-chloro-quinolin-6- yl)-vinyl]-4-nitro-thiophene-2-carboxylic acid methyl ester 7.7 (2.62 g, 82%) as an orange - red solid. TLC gradient Hex:EtOAc = 1 :1. MS: 375.70 (M+H+); 1H-NMR (DMSO-d6): δ (ppm) 8.50 (d, IH, J = 8.7 Hz), 8.34 (bs, IH), 8.18 (m, IH), 8.16 (bs, IH), 8.00 (d, IH, J = 9.0 Hz), 7.80 (d, IH, J = 16.5 Hz), 7.65 (d, IH, J = 8.7 Hz), 7.30 (d, IH, J = 17.4 Hz), 3.89 (s, 3H).
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