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[ CAS No. 13505-06-1 ] {[proInfo.proName]}

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Chemical Structure| 13505-06-1
Chemical Structure| 13505-06-1
Structure of 13505-06-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 13505-06-1 ]

CAS No. :13505-06-1 MDL No. :MFCD04114231
Formula : C5H4N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :BVXHEFWTMMZHDG-UHFFFAOYSA-N
M.W : 140.10 Pubchem ID :2762911
Synonyms :

Calculated chemistry of [ 13505-06-1 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 35.08
TPSA : 78.94 Ų

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) : -6.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.33
Log Po/w (XLOGP3) : 0.88
Log Po/w (WLOGP) : 0.7
Log Po/w (MLOGP) : -1.34
Log Po/w (SILICOS-IT) : -1.21
Consensus Log Po/w : -0.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.64
Solubility : 3.2 mg/ml ; 0.0229 mol/l
Class : Very soluble
Log S (Ali) : -2.12
Solubility : 1.06 mg/ml ; 0.00755 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.8
Solubility : 22.0 mg/ml ; 0.157 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.74

Safety of [ 13505-06-1 ]

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 [ 13505-06-1 ]

* 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 [ 13505-06-1 ]

[ 13505-06-1 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 13505-06-1 ]
  • [ 20443-98-5 ]
  • [ 66496-58-0 ]
YieldReaction ConditionsOperation in experiment
98.4% With caesium carbonate; In DMF (N,N-dimethyl-formamide); at 20.0℃; for 6.0h; To a stirred solution of Cs2CO3 (11. 63 G, 35. 69 MMOL) in DMF (180 mL) under a N2 atmosphere containing <strong>[13505-06-1]3-hydroxy-4-nitro-pyridine</strong> (5 G, 35. 69 MMOL) was added 2, 6-dichlorobenzyl bromide (8. 56 G, 35. 69 MMOI). The mixture was stirred for 6 h at ambient temperature. The reaction was then diluted with ETOAC (400 mL) and partitioned with H20 (100 ML). The aqueous layer was extracted with EtOAc (2 X 50 mL). The organic layers were then combined and washed with H20 (2 X 50 mL) and brine (1 X 50 mL). The organics were dried over NA2SO4, filtered and concentrated to dryness under vacuum to yield 3- (2, 6-DICHLORO-BENZYLOXY)-2-NITRO-PYRIDINE (10. 5 G, 98. 4%) as A white solid.
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