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[ CAS No. 29681-43-4 ] {[proInfo.proName]}

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Chemical Structure| 29681-43-4
Chemical Structure| 29681-43-4
Structure of 29681-43-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 29681-43-4 ]

CAS No. :29681-43-4 MDL No. :MFCD00956223
Formula : C8H9NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OJDKENGKKYVJLY-UHFFFAOYSA-N
M.W : 167.16 Pubchem ID :1519345
Synonyms :

Calculated chemistry of [ 29681-43-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.01
TPSA : 48.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.85
Log Po/w (XLOGP3) : 1.01
Log Po/w (WLOGP) : 0.88
Log Po/w (MLOGP) : 0.08
Log Po/w (SILICOS-IT) : 1.19
Consensus Log Po/w : 1.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.68
Solubility : 3.45 mg/ml ; 0.0207 mol/l
Class : Very soluble
Log S (Ali) : -1.62
Solubility : 4.05 mg/ml ; 0.0242 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.22
Solubility : 1.0 mg/ml ; 0.00601 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.81

Safety of [ 29681-43-4 ]

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

Application In Synthesis of [ 29681-43-4 ]

* 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 [ 29681-43-4 ]

[ 29681-43-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4437-20-1 ]
  • [ 29681-43-4 ]
  • [ 1450635-35-4 ]
YieldReaction ConditionsOperation in experiment
47% General procedure: Toa stirred solution of diisopropylamine (1.01mL, 7.18mmol) in dry THF (4 mL) wasadded n-butyllithium in hexane (1.6M in hexanes, (4.48 mL, 7.18 mmol) at -78 Cand stirred for 30 minutes at the same temperature. Methyl 4-methoxypicolinate(0.3g, 1.794mmol) in THF (3 mL) was added to the above solution and stirred forfurther 30 minutes at the same temperature. Disulfide 2a (0.53g, 2.15mmol) in THF (3 mL) was added at - 78oCand the mixture was stirred at the same temperature with continuous monitoringby TLC for 2h. Saturated NH4Cl solution (10 mL) was added to thereaction mixture and slowly warmed to room temperature and extracted with ethylacetate (3x25mL). The combined organic layer was dried over anhydrous Na2SO4and the volatiles were removed under reduced pressure. The resulting crudematerial was purified by column chromatography, eluting with 40% ethyl acetatein hexanes to afford compound 3a aspale yellow solid; Yield: 68%;
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