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[ CAS No. 351003-48-0 ] {[proInfo.proName]}

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Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 351003-48-0
Chemical Structure| 351003-48-0
Structure of 351003-48-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 351003-48-0 ]

CAS No. :351003-48-0 MDL No. :MFCD03094234
Formula : C6H3Cl2FO2S Boiling Point : -
Linear Structure Formula :- InChI Key :LIRQNYQIFFLGIE-UHFFFAOYSA-N
M.W : 229.06 Pubchem ID :2778321
Synonyms :

Calculated chemistry of [ 351003-48-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.49
TPSA : 42.52 ?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) : -5.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.75
Log Po/w (XLOGP3) : 2.67
Log Po/w (WLOGP) : 3.91
Log Po/w (MLOGP) : 2.54
Log Po/w (SILICOS-IT) : 2.44
Consensus Log Po/w : 2.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.25
Solubility : 0.13 mg/ml ; 0.000567 mol/l
Class : Soluble
Log S (Ali) : -3.21
Solubility : 0.14 mg/ml ; 0.00061 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.84
Solubility : 0.033 mg/ml ; 0.000144 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.05

Safety of [ 351003-48-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3265
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 351003-48-0 ]

* 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 [ 351003-48-0 ]

[ 351003-48-0 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 351003-48-0 ]
  • 2-amino-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid methyl ester hydrochloride [ No CAS ]
  • [ 904679-63-6 ]
  • 2
  • [ 351003-48-0 ]
  • [ 870249-31-3 ]
  • C25H33ClFN3O3S [ No CAS ]
  • C25H33ClFN3O3S [ No CAS ]
  • 3
  • [ 351003-48-0 ]
  • 2-[3-chloro-2-(3-diethylamino-propylamino)-benzenesulfonylamino]-5,6,7,8-tetrahydro-naphthalene-1-carboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
The following sulfonyl chlorides may be substituted for benzenesulfonyl chloride of Step One: ... 2-Chloro-4-fluorobenzenesulfonyl chloride 3-Chloro-4-fluorobenzenesulfonyl chloride 3-Chloro-2-fluorobenzenesulfonyl chloride 2-Chloro-6-methylbenzenesulfonyl chloride ...
  • 5
  • [ 351003-48-0 ]
  • [ 3306-62-5 ]
  • [ 1161943-96-9 ]
YieldReaction ConditionsOperation in experiment
19% With pyridine; for 12.0h; 2-Aminobenzenesulfonamide (54 mg, 0.31 mmol) and <strong>[351003-48-0]3-chloro-2-fluoro-benzenesulfonyl chloride</strong> (47 mg, 0.21 mmol) were dissolved in pyridine (1 ml) and the reaction mixture was stirred for 12 h. The solvent was removed in vacuo and the residue was purified by HPLC to give the product (15 mg, 19%).1H NMR (400 MHz, DMSO-d6) delta ppm 9.72 (br. s., 1H), 7.90 (t, 1H), 7.78-7.86 (m, 2H), 7.73 (br. s., 2H), 7.51-7.58 (m, 1H), 7.46-7.51 (m, 1H), 7.39 (t, 1H), 7.26-7.34 (m, 1H);MS m/z M-H 363.
  • 6
  • [ 351003-48-0 ]
  • [ 2930-05-4 ]
  • [ 100-46-9 ]
  • [ 1215721-21-3 ]
  • 7
  • [ 351003-48-0 ]
  • [ 1015170-94-1 ]
  • [ 1015168-91-8 ]
  • 8
  • [ 351003-48-0 ]
  • [ 1392442-82-8 ]
  • 9
  • [ 351003-48-0 ]
  • [ 1392441-83-6 ]
  • 10
  • [ 351003-48-0 ]
  • [ 100202-39-9 ]
  • [ 1392442-35-1 ]
  • 11
  • [ 351003-48-0 ]
  • 2C2HF3O2*C13H18N4O [ No CAS ]
  • [ 1392441-83-6 ]
  • 12
  • [ 351003-48-0 ]
  • [ 1380228-73-8 ]
  • [ 1380229-08-2 ]
YieldReaction ConditionsOperation in experiment
With pyridine; In dichloromethane; at 50℃; for 2.0h; The 2,6-difluoro-N1-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-yl)benzene-1,3-diamine(20 mg, 0.047 mmol) prepared at Step 9 was added and dissolved into dichloromethane solvent. <strong>[351003-48-0]3-chloro-2-fluorobenzene-1-sulfonyl chloride</strong> (16 mg, 0.07 mmol) and pyridine (8 uL, 0.094 mmol) were added into the reaction solution and stirred at 50C for 2 hours. After the reaction, the reactant was washed with 1N aqueous hydrochloric acid solution and salt water. After extraction with dichloromethane, the organic layer was dried with sulfuric anhydride magnesium and vacuum concentrated, and then refined by means of column chromatography, so that the target compound was obtained.1H NMR(400MHz, CDCl3): delta 11. 55 (s, 1H), 9.63(m, 1H), 8.99(d, J = 6.0 Hz, 1H), 8.39(d, J = 6.0 Hz, 1H), 8.20(s, 1H), 7.72(m, 1H), 7.61(m, 1H), 7.30(m, 1H), 7.18(m, 1H), 6.94(m, 2H), 5.91(m, 1H), 4.23(d, J = 11.2 Hz, 1H), 3.85(m, 1H), 2.19-1.72(m, 6H).
  • 13
  • [ 351003-48-0 ]
  • [ 351003-58-2 ]
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