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[ CAS No. 654073-32-2 ] {[proInfo.proName]}

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Chemical Structure| 654073-32-2
Chemical Structure| 654073-32-2
Structure of 654073-32-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 654073-32-2 ]

CAS No. :654073-32-2 MDL No. :MFCD18806627
Formula : C3H8N2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :STIUWSWFXIBBKI-UHFFFAOYSA-N
M.W : 136.17 Pubchem ID :45080566
Synonyms :

Calculated chemistry of [ 654073-32-2 ]

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 32.9
TPSA : 71.78 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.48
Log Po/w (XLOGP3) : -1.03
Log Po/w (WLOGP) : -0.4
Log Po/w (MLOGP) : -0.98
Log Po/w (SILICOS-IT) : -1.17
Consensus Log Po/w : -0.62

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.03
Solubility : 146.0 mg/ml ; 1.07 mol/l
Class : Highly soluble
Log S (Ali) : 0.01
Solubility : 139.0 mg/ml ; 1.02 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.42
Solubility : 357.0 mg/ml ; 2.62 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.81

Safety of [ 654073-32-2 ]

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 [ 654073-32-2 ]

* 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.

  • Upstream synthesis route of [ 654073-32-2 ]
  • Downstream synthetic route of [ 654073-32-2 ]

[ 654073-32-2 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 1271835-78-9 ]
  • [ 654073-32-2 ]
YieldReaction ConditionsOperation in experiment
58% With 2,5-dihydrotoluene; palladium(II) hydroxide In methanol at 60℃; Inert atmosphere A mixture of palladium hydroxide 20percent (350 mg), benzyl(azetidin-1-ylsulfonyl)carbamate (Preparation 20, 1 .49 g, 5.5 mmol) and 1-methyl-1,4-cyclohexadiene (10.7 g, 0.1 1 mol) in methanol (35 ml_) was stirred and heated at 60 °C overnight under nitrogen. The reaction mixture was cooled to room temperature, passed through a pad of celite and concentrated in vacuo to afford the title compound (437 mg, 58percent) as a solid. 1 H NMR (400 MHz, CD3OD) δ ppm 2.15 (pent, 2H), 3.78 (t, 4H). LCMS no mass ion observed
58% With 2,5-dihydrotoluene; palladium(II) hydroxide In methanol at 60℃; Inert atmosphere A mixture of palladium hydroxide 20percent (350 mg), benzyl (azetidin-l -ylsulfonyl)carbamate (Preparation 47, 1 .49 g, 5.5 mmol) and 1 -methyl-1 ,4-cyclohexadiene (10.7 g, 0.1 1 mol) in methanol (35 mL) was stirred and heated at 60 °C overnight under nitrogen. The reaction mixture was cooled to room temperature, passed through a pad of celite and concentrated in vacuo to afford the title compound (437 mg, 58percent) as a solid. 1 H NMR (400 MHz, CD3OD) δ ppm 2.15 (pent, 2H), 3.78 (t, 4H). MS m/z no mass ion observed
Reference: [1] Patent: WO2013/88315, 2013, A1, . Location in patent: Page/Page column 75
[2] Patent: WO2013/102826, 2013, A1, . Location in patent: Page/Page column 91
  • 2
  • [ 503-29-7 ]
  • [ 654073-32-2 ]
Reference: [1] Patent: WO2004/11443, 2004, A1, . Location in patent: Page 74-75
  • 3
  • [ 503-29-7 ]
  • [ 96042-30-7 ]
  • [ 654073-32-2 ]
Reference: [1] Patent: US2005/267018, 2005, A1,
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