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[ CAS No. 1828-66-6 ] {[proInfo.proName]}

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Chemical Structure| 1828-66-6
Chemical Structure| 1828-66-6
Structure of 1828-66-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1828-66-6 ]

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Product Details of [ 1828-66-6 ]

CAS No. :1828-66-6 MDL No. :MFCD03249981
Formula : C4H8ClNO3S Boiling Point : No data available
Linear Structure Formula :- InChI Key :KXIBCCFSAMRWIC-UHFFFAOYSA-N
M.W : 185.63 Pubchem ID :12798265
Synonyms :

Calculated chemistry of [ 1828-66-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.88
TPSA : 54.99 ?2

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) : -7.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.66
Log Po/w (XLOGP3) : -0.08
Log Po/w (WLOGP) : 0.5
Log Po/w (MLOGP) : -0.52
Log Po/w (SILICOS-IT) : 0.06
Consensus Log Po/w : 0.32

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.87
Solubility : 24.8 mg/ml ; 0.134 mol/l
Class : Very soluble
Log S (Ali) : -0.62
Solubility : 44.2 mg/ml ; 0.238 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.61
Solubility : 45.8 mg/ml ; 0.247 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.46

Safety of [ 1828-66-6 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310 UN#:3265
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1828-66-6 ]

* 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 [ 1828-66-6 ]

[ 1828-66-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1828-66-6 ]
  • [ 25999-04-6 ]
YieldReaction ConditionsOperation in experiment
270 mg With ammonium hydroxide; In water; acetone; at 0℃; for 2h; Morpholine-4-sulfonyl chloride (0.5 g, 4.3 mmol) in acetone (0.5 mL) was added to aq NH3 (1 .5 mL, NH4OH in H20, 28% NH3 basis) at 0 C and stirred at same temperature for 2 h. The solvent was removed in vacuo and the residue azeotroped twice with toluene. The residue was purified by column chromatography on silica gel using 2% MeOH-DCM eluent to give morpholine- 4-sulfonamide as white solid (270 mg, 60%). 1 H NMR (400 MHz, DMSO-d6): delta 6.82 (bs, 2H), 3.65 (t, J = 4.0 Hz, 4H), 2.92 (t, J = 4.0 Hz, 4H).
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