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[ CAS No. 1759-28-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1759-28-0
Chemical Structure| 1759-28-0
Structure of 1759-28-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1759-28-0 ]

CAS No. :1759-28-0 MDL No. :MFCD00005337
Formula : C6H7NS Boiling Point : -
Linear Structure Formula :- InChI Key :QUAMMXIRDIIGDJ-UHFFFAOYSA-N
M.W : 125.19 Pubchem ID :15654
Synonyms :

Calculated chemistry of [ 1759-28-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.17
TPSA : 41.13 ?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) : -5.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.89
Log Po/w (XLOGP3) : 2.16
Log Po/w (WLOGP) : 1.99
Log Po/w (MLOGP) : 0.75
Log Po/w (SILICOS-IT) : 3.23
Consensus Log Po/w : 2.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.37
Solubility : 0.53 mg/ml ; 0.00423 mol/l
Class : Soluble
Log S (Ali) : -2.66
Solubility : 0.276 mg/ml ; 0.00221 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.08
Solubility : 1.03 mg/ml ; 0.00824 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.17

Safety of [ 1759-28-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H227-H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1759-28-0 ]

* 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 [ 1759-28-0 ]

[ 1759-28-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 196929-85-8 ]
  • [ 1759-28-0 ]
  • [ 2942-16-7 ]
  • [ 1415338-18-9 ]
  • [ 1415338-20-3 ]
YieldReaction ConditionsOperation in experiment
57%; 55% At room temperature, (Rs) imine 2 (0.3 mmol) and the additive (0.315 mmol) was dissolved in 3 mL THF with vigorous stirring for about half an hour. The resulted clear solution was added to the priorly prepared benzothiazol-2-yl metallic reagent (0.45 mmol in 3 mL THF) at -78 C. The reaction was accomplished rapidly within 10 min (monitored by TLC). Then the reaction was quenched with aqueous saturated NH4Cl, extracted with DCM (10 mL × 3), washed by brine (10 mL), dried over Na2SO4, and concentrated under vacuum. The crude product was purified by silica gel column chromatography (petroleum ether/ethyl acetate 3:1-1:1). The diastereoselectivity was determined by 1H NMR analysis of the crude product.
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