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[ CAS No. 150-78-7 ] {[proInfo.proName]}

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Chemical Structure| 150-78-7
Chemical Structure| 150-78-7
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Product Details of [ 150-78-7 ]

CAS No. :150-78-7 MDL No. :MFCD00008401
Formula : C8H10O2 Boiling Point : -
Linear Structure Formula :(CH3O)2(C6H4) InChI Key :OHBQPCCCRFSCAX-UHFFFAOYSA-N
M.W : 138.16 Pubchem ID :9016
Synonyms :

Calculated chemistry of [ 150-78-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.43
TPSA : 18.46 ?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) : -5.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.16
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 1.7
Log Po/w (MLOGP) : 1.48
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 1.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.29
Solubility : 0.702 mg/ml ; 0.00508 mol/l
Class : Soluble
Log S (Ali) : -2.06
Solubility : 1.22 mg/ml ; 0.00879 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.62
Solubility : 0.329 mg/ml ; 0.00238 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 150-78-7 ]

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 [ 150-78-7 ]

* 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 [ 150-78-7 ]
  • Downstream synthetic route of [ 150-78-7 ]

[ 150-78-7 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 150-78-7 ]
  • [ 53581-81-0 ]
Reference: [1] Journal of Medicinal Chemistry, 1975, vol. 18, # 12, p. 1201 - 1204
  • 2
  • [ 68-12-2 ]
  • [ 150-78-7 ]
  • [ 5312-97-0 ]
YieldReaction ConditionsOperation in experiment
92%
Stage #1: With n-butyllithium In tetrahydrofuran; hexane at 0℃; for 2 h;
Stage #2: at 0℃; for 2 h;
Stage #3: With ammonia; iodine In tetrahydrofuran; hexane; water at 0 - 20℃; for 2 h;
General procedure: n-Butyllithium (1.67 M solution in hexane, 2.9 mL, 4.8 mmol) was added dropwise into a solution of 1,3-dimethoxybenzene (0.55 g, 4.0 mmol) in THF (5 mL) at 0 °C and the mixture was stirred for 2 h at the same temperature. Then, DMF (0.34 mL, 4.4 mmol) was added to the mixture and the obtained mixture was stirred at 0 °C. After 2 h at the same temperature, aq NH3 (8 mL, 120 mmol) and I2 (1.12 g, 4.4 mmol) were added and stirred for 2 h at rt. The reaction mixture was quenched with satd aq Na2SO3 (15 mL) and was extracted with Et2O (3.x.20 mL). The organic layer was washed with brine and dried over Na2SO4 to provide 2,6-dimethoxybenzonitrile in over 80percent purity. The product was purified by a short column chromatography on silica gel (Hexane/EtOAc=3:1) to give pure 2,6-dimethoxybenzonitrile in 91percent yield as a colorless solid.
Reference: [1] Synlett, 2010, # 10, p. 1562 - 1566
[2] Tetrahedron, 2011, vol. 67, # 5, p. 958 - 964
  • 3
  • [ 93-61-8 ]
  • [ 150-78-7 ]
  • [ 5312-97-0 ]
YieldReaction ConditionsOperation in experiment
71%
Stage #1: at 0℃; for 0.5 h;
Stage #2: at 100℃; for 10 h;
Stage #3: With ammonia; iodine In tetrahydrofuran; water; N,N-dimethyl-formamide at 20℃; for 3 h;
General procedure: To an ice cooled solution of N-methylformanilide (2.2 mmol) was added dropwise diphosphoryl chloride (2.2 mmol). The solution was stirred for 30 min at 0 °C, and then 1,2-dimethoxybenzene (276.3 mg, 2 mmol) in DMF (1.0 mL) was added dropwise. After being stirred for 10 h at 100 °C, I2 (1015.2 mg, 4 mmol), aq NH3 (4 mL, 28-30percent) and THF (1 mL) were added to the reaction mixture. The obtained mixture was stirred for 3 h at rt. After the reaction, the mixture was poured into aq satd Na2SO3 solution and extracted with CHCl3 (3.x.20 mL). The organic layer was dried over Na2SO4, filtered, and evaporated. The product was purified by flash short column chromatography (Hexane:AcOEt=3:1) to afford 3,4-dimethoxybenzonitrile as a white solid in 92percent yield.
Reference: [1] Tetrahedron, 2012, vol. 68, # 24, p. 4588 - 4595
  • 4
  • [ 150-78-7 ]
  • [ 5312-97-0 ]
Reference: [1] Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1983, vol. 38, # 7, p. 866 - 872
[2] Justus Liebigs Annalen der Chemie, 1906, vol. 344, p. 46[3] Chemische Berichte, 1905, vol. 38, p. 796
  • 5
  • [ 506-68-3 ]
  • [ 150-78-7 ]
  • [ 5312-97-0 ]
Reference: [1] Helvetica Chimica Acta, 1920, vol. 3, p. 266
  • 6
  • [ 143-33-9 ]
  • [ 150-78-7 ]
  • [ 5312-97-0 ]
  • [ 874-90-8 ]
Reference: [1] Bulletin de la Societe Chimique de France, 1989, # 2, p. 156 - 167
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