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[ CAS No. 1014-25-1 ] {[proInfo.proName]}

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Chemical Structure| 1014-25-1
Chemical Structure| 1014-25-1
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Product Details of [ 1014-25-1 ]

CAS No. :1014-25-1 MDL No. :MFCD00813220
Formula : C9H9N3OS Boiling Point : -
Linear Structure Formula :- InChI Key :UJBCFMCQLVRXBQ-UHFFFAOYSA-N
M.W : 207.25 Pubchem ID :692882
Synonyms :

Calculated chemistry of [ 1014-25-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.11
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 56.24
TPSA : 89.27 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.84
Log Po/w (XLOGP3) : 1.65
Log Po/w (WLOGP) : 1.8
Log Po/w (MLOGP) : 0.94
Log Po/w (SILICOS-IT) : 2.41
Consensus Log Po/w : 1.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.61
Solubility : 0.504 mg/ml ; 0.00243 mol/l
Class : Soluble
Log S (Ali) : -3.14
Solubility : 0.151 mg/ml ; 0.000728 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.21
Solubility : 0.127 mg/ml ; 0.000611 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 1014-25-1 ]

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

Application In Synthesis of [ 1014-25-1 ]

* 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 [ 1014-25-1 ]

[ 1014-25-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1014-25-1 ]
  • [ 110677-45-7 ]
  • C28H20N4OS [ No CAS ]
YieldReaction ConditionsOperation in experiment
80.43% In ethanol; at 70℃; for 12h; T1 (0.271 g, 1 mmol) and compound 1 (0.248 g, 1.2 mmol) weredissolved in 15 mL of anhydrous alcohol, the reaction mixture wasrefluxed at 70 C for 12 h. After the reaction finished, the solutionwas cooled to room temperature, the solid was filtered and washedtwo times with anhydrous ethanol to give 0.37 g green solid, yield:80.43%. Melting point: 217.4-218.5 C. FT- IR (KBr, Disc, cm1):1601.19 (s, ν CN), 1582.00 (m), 1558.11 (m), 1514.46 (s, νbenzene),1445.05 (s), 1417.20 (m), 1360.58 (m), 1337.06 (m), 1312.98 (w),1252.84 (m), 1224.75 (m, νOCH3), 1178.97 (m, ν OCH3), 1159.28 (m,ν OCH3), 825.46 (m), 737.66 (m), 718.23 (m). 1H NMR (DMSO-d6,400 MHz, ppm) δ: 9.20 (s, 1H, CHN), 8.38-8.36 (d, J = 8.0 Hz, 2H),8.30-8.28 (d, J =8.0 Hz, 2H), 7.98-7.91 (q, 4H), 7.58-7.56 (d,J =8.0 Hz, 2H), 7.51-7.48 (t, 2H), 7.37-7.34 (t, 2H), 7.16-7.14 (d,J = 8.0 Hz, 2H), 3.85 (s, 3H, OCH3). 13C NMR (100 MHz, CDCl3)δ 172.83,167.39,165.10,162.03,142.39,140.16,133.11,131.72,129.25,126.89, 126.27, 123.95, 123.25, 120.74, 120.49, 114.59, 109.86, 55.50.MS (ESI) m/z: found, [M+H]+, 461.1427; molecular formulaC28H20N4OS requires [M+H]+, 461.1436.
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