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[ CAS No. 39070-14-9 ] {[proInfo.proName]}

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Chemical Structure| 39070-14-9
Chemical Structure| 39070-14-9
Structure of 39070-14-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 39070-14-9 ]

CAS No. :39070-14-9 MDL No. :MFCD06738747
Formula : C5H7N3O3 Boiling Point : -
Linear Structure Formula :- InChI Key :WXSSUDRHAJTESR-UHFFFAOYSA-N
M.W : 157.13 Pubchem ID :70292
Synonyms :

Calculated chemistry of [ 39070-14-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.4
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.44
TPSA : 83.87 ?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) : -7.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.43
Log Po/w (XLOGP3) : -0.35
Log Po/w (WLOGP) : -0.33
Log Po/w (MLOGP) : -1.16
Log Po/w (SILICOS-IT) : -1.89
Consensus Log Po/w : -0.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.8
Solubility : 25.0 mg/ml ; 0.159 mol/l
Class : Very soluble
Log S (Ali) : -0.95
Solubility : 17.7 mg/ml ; 0.112 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.01
Solubility : 159.0 mg/ml ; 1.01 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.19

Safety of [ 39070-14-9 ]

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

Application In Synthesis of [ 39070-14-9 ]

* 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 [ 39070-14-9 ]

[ 39070-14-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3107-19-5 ]
  • [ 39070-14-9 ]
  • 2-(2,6-dichloro-4-nitrophenoxymethyl)-1-methyl-5-nitro-1H-imidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃;Heating; A mixture of 2-( 1 -methyl-5-nitro- 1 H-imidazol-2-yl)-ethanol (1.15 mmol) and 1 ,3- dichloro-2-fluoro-5-nitro-benzene (1.24 mmol) and K2C03(465 mg, 3.36 mmol) in DMF (5 mL) was stirred 2 hours at ambient temperature followed by heating. The reaction was worked-up by extraction. The residue was purified by prep-HPLC with the following condition: column:XBridge preparative C18 OBD column 19x150 mm, 5 um; mobile phase A: water (10 mmol/L NH4HC03), mobile phase B: ACN; flow rate: 20 mL/min; gradient elution. The product- containing fractions were collected and then lyophilized to give 2-(2,6-dichloro-4-nitro- phenoxymethyl)-l-methyl-5-nitro-lH-imidazole. LC-MS: (ES, m/z) 346. (M+H)+; analysis: C, 38.01; H, 2.22; CI, 20.13; N, 16.19; O, 23.15.
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