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[ CAS No. 7312-11-0 ] {[proInfo.proName]}

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Chemical Structure| 7312-11-0
Chemical Structure| 7312-11-0
Structure of 7312-11-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 7312-11-0 ]

CAS No. :7312-11-0 MDL No. :MFCD05662034
Formula : C10H7BrO2S Boiling Point : -
Linear Structure Formula :- InChI Key :XDYVZHUZZZKQOS-UHFFFAOYSA-N
M.W : 271.13 Pubchem ID :2824065
Synonyms :

Calculated chemistry of [ 7312-11-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 60.8
TPSA : 54.54 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.75
Log Po/w (XLOGP3) : 3.82
Log Po/w (WLOGP) : 3.45
Log Po/w (MLOGP) : 2.96
Log Po/w (SILICOS-IT) : 4.14
Consensus Log Po/w : 3.42

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.27
Solubility : 0.0145 mg/ml ; 0.0000535 mol/l
Class : Moderately soluble
Log S (Ali) : -4.66
Solubility : 0.00592 mg/ml ; 0.0000218 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.27
Solubility : 0.0145 mg/ml ; 0.0000536 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 7312-11-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 7312-11-0 ]

* 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 [ 7312-11-0 ]

[ 7312-11-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 126-33-0 ]
  • [ 7312-11-0 ]
  • methyl 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
26% Intermediate 14) Synthesis of 5-(l,l-dioxidotetrahydrothiophen-2- yl)benzo[6]thiophene-2-carboxylic acid (a) Synthesis of methyl 5-(l,l-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene- 2-carboxylate Tetrahydrothiophene 1,1 -dioxide (124.0 mg, 1.03 mmol) was dissolved in anhydrous THF (7.3 mL), and 1M solution of lithium bis(trimethylsilyl)amide in THF (1.5 mL, 1.55 mmol) was added dropwise at -20C. The reaction mixture was stirred at room temperature for 30 minutes, and ZnCl2 (211.0 mg, 1.55 mmol) was added -20C. The reaction mixture was slowly warmed to room temperature, methyl 5- bromobenzo[b]thiophene-2-carboxylate (200.0 mg, 0.74 mmol), Pd(OAc)2 (8.3 mg, 0.04 mmol) and XPhos (35.2 mg, 0.07 mmol) were added, and stirred at 65C for 5 hours. The reaction mixture was cooled to room temperature, H20 was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na2S04 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex : EtOAc = 9 : 1) to obtain methyl 5-(l,l- dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylate (60.0 mg, 26%) as an off-white solid. 1H-NMR (400MHz, CDC13): delta 8.06 (s, 1H), 7.89-7.91 (m, 2H), 7.49 (dd, 1H, J=8.4, 2.0Hz), 4.30 (m, 1H), 3.95 (s, 3H), 2.95-3.35 (m, 3H), 2.22-2.58 (m, 3H)
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