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[ CAS No. 5785-70-6 ] {[proInfo.proName]}

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Chemical Structure| 5785-70-6
Chemical Structure| 5785-70-6
Structure of 5785-70-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5785-70-6 ]

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Product Details of [ 5785-70-6 ]

CAS No. :5785-70-6 MDL No. :MFCD02179460
Formula : C9H10BNO6 Boiling Point : -
Linear Structure Formula :- InChI Key :GCDAYMSNTGTFDC-UHFFFAOYSA-N
M.W : 238.99 Pubchem ID :2773403
Synonyms :

Calculated chemistry of [ 5785-70-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 5
Num. H-bond acceptors : 6.0
Num. H-bond donors : 2.0
Molar Refractivity : 61.18
TPSA : 112.58 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.14 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.87
Log Po/w (WLOGP) : -0.55
Log Po/w (MLOGP) : -0.45
Log Po/w (SILICOS-IT) : -2.58
Consensus Log Po/w : -0.54

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.8
Solubility : 3.78 mg/ml ; 0.0158 mol/l
Class : Very soluble
Log S (Ali) : -2.82
Solubility : 0.363 mg/ml ; 0.00152 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.16
Solubility : 16.6 mg/ml ; 0.0697 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.46

Safety of [ 5785-70-6 ]

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 [ 5785-70-6 ]

* 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 [ 5785-70-6 ]

[ 5785-70-6 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 57362-77-3 ]
  • [ 5785-70-6 ]
  • 2
  • [ 5785-70-6 ]
  • [ 935433-66-2 ]
YieldReaction ConditionsOperation in experiment
65% A solution of methyl 2-(bromomethyl)benzoate (261 mg, 1.14 mmol) and tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.045 mmol) in DME (2 mL) under argon was stirred at room temperature for lOmin. 4-Ethoxycarbonyl-2-nitrophenylboronic acid (308 mg, 1.29 mmol) dissolved in DME/EtOH 2:1 (3 mL) was added followed by 2M aq. Na2CO3 (2 mL) and stirring was continued for 2h. The reaction mixture was concentrated in vacuo and purified by column chromatography using EtOAc (0-10%) in heptane as the eluent furnishing 338 mg of 4-(2-Methoxycarbonyl-benzyl)-3-nitro-benzoic acid ethyl ester as a colorless solid (1.13 mmol, 65%).[0246] 1H NMR (400MHz, CDCl3): 8.58 (d, 2H), 8.06 (dd, IH), 8.02 (dd, 2H), 7.50 (dt, IH), 7.38 (dt, IH), 7.18 (d, IH), 7.06 (d, IH), 4.69 (s, 2H), 4.39 (q, 2H), 3.76 (s, 3H), 1.40 (t, 3H).
  • 3
  • [ 2417-73-4 ]
  • [ 5785-70-6 ]
  • [ 935433-66-2 ]
YieldReaction ConditionsOperation in experiment
65% A solution of methyl 2-(bromomethyl)benzoate (261 mg, 1.14 mmol) and tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.045 mmol) in DME (2 mL) under argon was stirred at room temperature for lOmin. 4-Ethoxycarbonyl-2-nitrophenylboronic acid (308 mg, 1.29 mmol) dissolved in DME/EtOH 2:1 (3 mL) was added followed by 2M aq. Na2CO3 (2 mL) and stirring was continued for 2h. The reaction mixture was <n="103"/>concentrated in vacuo and purified by column chromatography using EtOAc (0-10%) in heptane as the eluent furnishing 338 mg of 4-(2-Methoxycarbonyl-benzyl)-3-nitro- benzoic acid ethyl ester as a colorless solid (1.13 mmol, 65%).[0327] 1H NMR (400MHz, CDCl3): 8.58 (d, 2H), 8.06 (dd, 1H), 8.02 (dd,2H), 7.50 (dt, 1H), 7.38 (dt, 1H), 7.18 (d, 1H), 7.06 (d, 1H), 4.69 (s, 2H), 4.39 (q, 2H), 3.76 (s, 3H), 1.40 (t, 3H).
65% A solution of methyl 2-(bromomethyl)benzoate (261mg, 1.14mmol) and tetrakis(triphenylphosphine)palladium(0) (52mg,0.045mmol) in DME (2mL) under argon was stirred at room temperature for lOmin. 4-Ethoxycarbonyl-2-nitrophenylboronic acid (308mg, 1.29mmol) dissolved in DME/EtOH 2:1 (3mL) was added followed by 2M aq. Na2CO3 (2mL) and stirring was continued for 2h. The reaction mixture was concentrated in vacuo and purified by column chromatography using EtOAc (0-10%) in heptane as the eluent EPO <DP n="85"/>furnishing 338 nig of xxl as a colourless solid (1.13mmol, 65%). 1H NMR (400MHz, CDCl3): 8.58 (d, 2H), 8.06 (dd, IH), 8.02 (dd, 2H), 7.50 (dt, IH), 7.38 (dt, IH), 7.18 (d, IH), 7.06 (d, IH), 4.69 (s, 2H), 4.39 (q, 2H), 3.76 (s, 3H), 1.40 (t, 3H).
  • 4
  • [ 7115-89-1 ]
  • [ 5785-70-6 ]
  • [ 935433-66-2 ]
  • 5
  • [ 5785-70-6 ]
  • [ 33515-09-2 ]
  • C64H82N18O17 [ No CAS ]
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