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[ CAS No. 1197-13-3 ] {[proInfo.proName]}

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Chemical Structure| 1197-13-3
Chemical Structure| 1197-13-3
Structure of 1197-13-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1197-13-3 ]

CAS No. :1197-13-3 MDL No. :MFCD09878545
Formula : C7H7NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PRCYHYGREGWAAN-UHFFFAOYSA-N
M.W : 153.14 Pubchem ID :316531
Synonyms :

Calculated chemistry of [ 1197-13-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.14
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 37.46
TPSA : 59.16 ?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) : -6.74 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.46
Log Po/w (XLOGP3) : 0.69
Log Po/w (WLOGP) : 0.61
Log Po/w (MLOGP) : -0.57
Log Po/w (SILICOS-IT) : 1.39
Consensus Log Po/w : 0.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.36
Solubility : 6.65 mg/ml ; 0.0434 mol/l
Class : Very soluble
Log S (Ali) : -1.51
Solubility : 4.74 mg/ml ; 0.0309 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.62
Solubility : 3.71 mg/ml ; 0.0242 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.72

Safety of [ 1197-13-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1197-13-3 ]

* 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 [ 1197-13-3 ]

[ 1197-13-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1197-13-3 ]
  • [ 937-19-9 ]
YieldReaction ConditionsOperation in experiment
Ca. 71% NH2OH·HCl (0.58 g, 8.4 mmol) and NaOAc (0.63 g, 7.6 mmol) were added to a solution of methyl 5-formyl-1H-pyrrole-2-carboxylate 12 (1.14 g, 7.6 mmol) in anhydrous MeOH (8 mL), and the mixture was heated at the reflux temperature for 1 h. The resulting solution was quenched with NaHCO3 aq, and the aqueous layer was extracted with CH2Cl2 for three times. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo to give the corresponding aldoxime (1.11 g, <87%). The crude oxime (5.8 g, 34 mmol) thus obtained was dissolved in anhydrous N,N-dimethylformamide (DMF, 28 mL), and the solution was added dropwise POCl3 (8.4 g, 55 mmol) at -20 C. After being stirred for 30 min at -20 C and then at rt for 2 h, the reaction was quenched with water. The aqueous layer was extracted with CH2Cl2 for three times. The combined organic layers were washed with water for five times, dried over anhydrous MgSO4, and concentrated in vacuo to give the title compound (4.2 g, ~71%) as a colorless solid (mp=173.7-174.8 C), Rf 0.23 (hexane/ethyl acetate=3:1). 1H NMR (400 MHz, CDCl3) δ 9.92 (br, 1H), 6.89 (dd, J=3.9, 2.5 Hz, 1H), 6.84 (dd, J=4.0, 2.6 Hz, 1H), 3.94 (s, 3H); 13C NMR (101 MHz, CDCl3) δ 160.9, 126.7, 120.1, 115.2, 112.8, 105.7, 52.7; HRMS (EI) calcd for C7H6N2O2: M+, 150.0429. Found: m/z 150.0430.
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