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[ CAS No. 701-57-5 ] {[proInfo.proName]}

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Chemical Structure| 701-57-5
Chemical Structure| 701-57-5
Structure of 701-57-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 701-57-5 ]

CAS No. :701-57-5 MDL No. :MFCD00010868
Formula : C7H7NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :NEZGPRYOJVPJKL-UHFFFAOYSA-N
M.W : 169.20 Pubchem ID :96109
Synonyms :

Calculated chemistry of [ 701-57-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.99
TPSA : 71.12 ?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) : -5.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.43
Log Po/w (XLOGP3) : 2.58
Log Po/w (WLOGP) : 2.32
Log Po/w (MLOGP) : 1.46
Log Po/w (SILICOS-IT) : 0.22
Consensus Log Po/w : 1.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.79
Solubility : 0.277 mg/ml ; 0.00164 mol/l
Class : Soluble
Log S (Ali) : -3.72
Solubility : 0.0321 mg/ml ; 0.00019 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.27
Solubility : 0.909 mg/ml ; 0.00537 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 701-57-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P501 UN#:
Hazard Statements:H302+H312+H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 701-57-5 ]

* 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 [ 701-57-5 ]

[ 701-57-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 701-57-5 ]
  • [ 65938-77-4 ]
  • [ 960008-46-2 ]
YieldReaction ConditionsOperation in experiment
54% With [bis(acetoxy)iodo]benzene; magnesium oxide;dirhodium tetraacetate; In dichloromethane; at 20℃; for 24h; (RS)-S-Methyl-S-(4-nitrophenyl)-N-[(5-methyl-2-pyridyl)sulphonyl]sulphimide 879 mg (2.73 mmol) of iodosobenzene diacetate are added to a suspension of 300 mg (1.77 mmol) of 1-methylsulphanyl-4-nitrobenzene, 610 mg (3.55 mmol) of 5-methyl-2-pyridinesulphonamide, 285 mg (7.10 mmol) of magnesium oxide and 78 mg (0.18 mmol) of rhodium(II) acetate dimer in 12 ml of dichloromethane at room temperature. The mixture is stirred for 24 h and then concentrated. The resulting residue is purified by chromatography (dichloromethane/ethanol 95:5). 326 mg (0.96 mmol; yield: 54%) of the product are obtained. 1H-NMR (DMSO): 8.41 (m, 2H), 8.31 (m, 1H), 8.12 (m, 2H), 7.76 (m, 1H), 7.70 (m, 1H), 3.11 (s, 3H), 2.29 (s, 3H). MS: 340 (ES+).
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