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[ CAS No. 27329-70-0 ] {[proInfo.proName]}

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Chemical Structure| 27329-70-0
Chemical Structure| 27329-70-0
Structure of 27329-70-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 27329-70-0 ]

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Product Details of [ 27329-70-0 ]

CAS No. :27329-70-0 MDL No. :MFCD01114696
Formula : C5H5BO4 Boiling Point : -
Linear Structure Formula :HCOC4H2OB(OH)2 InChI Key :JUWYQISLQJRRNT-UHFFFAOYSA-N
M.W : 139.90 Pubchem ID :2734355
Synonyms :

Calculated chemistry of [ 27329-70-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 33.92
TPSA : 70.67 ?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) : -7.35 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -0.28
Log Po/w (WLOGP) : -1.23
Log Po/w (MLOGP) : -2.29
Log Po/w (SILICOS-IT) : -1.09
Consensus Log Po/w : -0.98

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.77
Solubility : 23.8 mg/ml ; 0.17 mol/l
Class : Very soluble
Log S (Ali) : -0.74
Solubility : 25.2 mg/ml ; 0.18 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.42
Solubility : 52.8 mg/ml ; 0.378 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.56

Safety of [ 27329-70-0 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P362+P364-P403+P233-P501 UN#:3077
Hazard Statements:H315-H318-H335-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 27329-70-0 ]

* 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 [ 27329-70-0 ]

[ 27329-70-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 13195-50-1 ]
  • [ 27329-70-0 ]
  • 5-(5-nitrothiophen-2-yl)-furan-2-carbaldehyde [ No CAS ]
  • 2
  • [ 27329-70-0 ]
  • [ 42860-10-6 ]
  • [ 425630-53-1 ]
  • 3
  • [ 27329-70-0 ]
  • [ 3032-81-3 ]
  • [ 106827-27-4 ]
YieldReaction ConditionsOperation in experiment
89% With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; In 1,2-dimethoxyethane; ethanol; water; at 65℃; for 1h; General procedure: 1.00 mmol arylhalide, 1.30 mmol furfural-boronic acid and 0.05 mmolBis(triphenylphosphine)palladium(II) dichloride were treated with 0.30 mLdimethoxyethane, 0.50 mL ethanol and 0.30 mL aqueous 2M sodium carbonate solution.The reaction was heated to 65°C for 1h or until the TLC showed no remaining startingmaterial. The mixture was evaporated and extracted three times with ethyl acetate. Thecombined organic layers were washed with brine, dried over MgSO4, filtered andconcentrated. The crude product was purified by column chromatography usinghexanes/ethyl acetate (9:1).
  • 4
  • [ 27329-70-0 ]
  • [ 2401-21-0 ]
  • 5-(2',3'-dichlorophenyl)furan-2-carbaldehyde [ No CAS ]
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