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[ CAS No. 1400764-35-3 ] {[proInfo.proName]}

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Chemical Structure| 1400764-35-3
Chemical Structure| 1400764-35-3
Structure of 1400764-35-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1400764-35-3 ]

CAS No. :1400764-35-3 MDL No. :MFCD22421657
Formula : C4H6ClN3 Boiling Point : -
Linear Structure Formula :- InChI Key :JFYVVPPBUPKQEN-UHFFFAOYSA-N
M.W : 131.56 Pubchem ID :72208258
Synonyms :

Calculated chemistry of [ 1400764-35-3 ]

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.4
TPSA : 51.8 Ų

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) : -6.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.27
Log Po/w (WLOGP) : 0.87
Log Po/w (MLOGP) : -0.31
Log Po/w (SILICOS-IT) : 0.38
Consensus Log Po/w : 0.24

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.38
Solubility : 5.47 mg/ml ; 0.0416 mol/l
Class : Very soluble
Log S (Ali) : -0.92
Solubility : 15.8 mg/ml ; 0.12 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.21
Solubility : 8.21 mg/ml ; 0.0624 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.64

Safety of [ 1400764-35-3 ]

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 [ 1400764-35-3 ]

* 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 [ 1400764-35-3 ]

[ 1400764-35-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1400764-35-3 ]
  • [ 1885-14-9 ]
  • [ 115136-48-6 ]
YieldReaction ConditionsOperation in experiment
68% With pyridine In tetrahydrofuran; acetonitrile at 0℃; for 12h; 57.1 Step-1: phenyl pyridazin-4-ylcarbamate To a solution of pidazin-4-amine hydrochloride (0.090 g, 0.680 mmol) and pidine(0.120 g, 1.500 mmol) in acetonitrile:THF (1:1) (10 mL) was added phenylchloroformate(0.090 mL, 0.750 mmol) at 0 °C. The reaction mixture was stirred for 12 h. The reaction mixtures was diluted with water (50 mL) and extracted with ethyl acetate (2 x 50 mL). The combined organic layer was dried over sodium sulfate and evaporated under reduced pressure to give a residue. The residue was purified by column chromatography (ethylacetate/hexanes = 60/40) to give the titled compound (0.100 g, 68 %) as a solid.
68% With pyridine In tetrahydrofuran; acetonitrile at 0 - 20℃; for 12h; 18.1 Step-1 : phenyl(pyridazin-4-yl)carbamate To a solution of pyridazin-4-amine hydrochloride (0.090 g, 0.680 mmol) and pyridine (0.120 g, 1.500 mmol) in acetonitrile:THF (1 :1) (10 mL) was added phenylchloroformate (0.090 mL, 0.750 mmol) at 0 °C. The above reaction mixture was stirred for 12 h at room temperature. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (2 x 50 mL). The combined organic layer was dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (ethyl acetate/hexanes = 60/40) to afford the title compound (0.100 g, 68 %) as a solid.
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