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[ CAS No. 31680-07-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 31680-07-6
Chemical Structure| 31680-07-6
Structure of 31680-07-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 31680-07-6 ]

CAS No. :31680-07-6 MDL No. :MFCD00017011
Formula : C8H7NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KHWGAWBXQOKXIJ-UHFFFAOYSA-N
M.W : 165.15 Pubchem ID :1798998
Synonyms :

Calculated chemistry of [ 31680-07-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.62
TPSA : 62.89 ?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) : -5.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.26
Log Po/w (XLOGP3) : 1.88
Log Po/w (WLOGP) : 1.72
Log Po/w (MLOGP) : 0.59
Log Po/w (SILICOS-IT) : 0.28
Consensus Log Po/w : 1.14

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 : 0.854 mg/ml ; 0.00517 mol/l
Class : Soluble
Log S (Ali) : -2.82
Solubility : 0.248 mg/ml ; 0.0015 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.11
Solubility : 1.29 mg/ml ; 0.00783 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.69

Safety of [ 31680-07-6 ]

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

Application In Synthesis of [ 31680-07-6 ]

* 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 [ 31680-07-6 ]

[ 31680-07-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31680-07-6 ]
  • [ 13338-63-1 ]
  • [ 5137-55-3 ]
  • [ 162705-18-2 ]
YieldReaction ConditionsOperation in experiment
14.1% With sodium hydroxide; In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; dichloromethane; water; Step 1 Preparation of (Z)-3-(3-nitro-4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-ene-nitrile 5.0 g of 3-nitro-4-methylbenzaldehyde, 6.27 g of <strong>[13338-63-1]3,4,5-trimethoxyphenylacetonitrile</strong>, 1.44 g of sodium hydroxide and 500 mg of trioctylmethylammonium chloride were dissolved in 25 ml of water and 500 ml of dichloromethane. The mixture was stirred vigorously for 3 hours at room temperature. The ice water was added to the mixture and the mixture was extracted with dichloromethane three times and dried over anhydrous sodium sulfate. The organic layer was concentrated and the residue was purified by silica gel column chromatography (dichloromethane) to give 1.5 g of the intended compound. The yield was 14.1%. 1 H-NMR(CDCl3): 8.35 (1H, J=1.5), 8.18 (1H, dd, J=1.5, 8.1), 7.47 (1H, d, J=8.1), 7.44 (1H, s), 6.88 (2H, s), 3.95 (6H, s), 3.90 (3H, s), 2.67 (3H, s); mass spectrum (m/z): 354 (M+); melting point 162-163 C.
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