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[ CAS No. 389-58-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 389-58-2
Chemical Structure| 389-58-2
Structure of 389-58-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 389-58-2 ]

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Product Details of [ 389-58-2 ]

CAS No. :389-58-2 MDL No. :MFCD20133900
Formula : C9H6S2 Boiling Point : -
Linear Structure Formula :- InChI Key :UITASDKJJNYORO-UHFFFAOYSA-N
M.W : 178.27 Pubchem ID :136232
Synonyms :

Calculated chemistry of [ 389-58-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.11
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.64
TPSA : 56.48 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.32
Log Po/w (XLOGP3) : 2.98
Log Po/w (WLOGP) : 3.38
Log Po/w (MLOGP) : 2.69
Log Po/w (SILICOS-IT) : 5.37
Consensus Log Po/w : 3.35

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.5
Solubility : 0.057 mg/ml ; 0.00032 mol/l
Class : Soluble
Log S (Ali) : -3.83
Solubility : 0.0264 mg/ml ; 0.000148 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.72
Solubility : 0.0338 mg/ml ; 0.00019 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.64

Safety of [ 389-58-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 389-58-2 ]

* 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.

  • Downstream synthetic route of [ 389-58-2 ]

[ 389-58-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25796-77-4 ]
  • [ 389-58-2 ]
YieldReaction ConditionsOperation in experiment
66% With potassium hydroxide; hydrazine; In ethylene glycol; at 190℃; for 13h; <Synthesis of compound K> After placing compound (77) (96 mg, 0.499 mmol), hydrazine monohydrate (268 mg, 5.35 mmol), potassium hydroxide (294 mg, 5.249 mmol) and ethylene glycol (5 mL) in a heat-dried stoppered test tube, the mixture was slowly heated from room temperature to 190°C and then refluxed at 190°C for 13 hours. After then cooling the mixture to room temperature, water was added and the organic phase was extracted with ether. The organic phase was washed with water and brine and dried over magnesium sulfate, and concentrated under reduced pressure. It was then purified by silica gel column chromatography (hexane:ethyl acetate = 10:1) to obtain the target compound K (59 mg, 66percent yield) as a white solid. The analysis results and chemical formula for the obtained compound K are shown below. Upon measuring the obtained compound K by CV, the oxidation potential was 0.68 V and the reduction potential was -2.88 V. The peak wavelength in the absorption spectrum of compound K was 310 nm. TLC Rf = 0.7 (hexane: CH2Cl2 = 2 :1): 1H NMR (270 MHz, CDCl3): delta 7.17 (d, 2H, J = 4.8 Hz), 7.09 (d, 2H, J = 4.8 Hz), 3.54 (s, 2H): GC-MS (EI): m/z = 178 (M+).
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