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[ CAS No. 2863-98-1 ] {[proInfo.proName]}

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Chemical Structure| 2863-98-1
Chemical Structure| 2863-98-1
Structure of 2863-98-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2863-98-1 ]

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Product Details of [ 2863-98-1 ]

CAS No. :2863-98-1 MDL No. :MFCD00673994
Formula : C7H8ClN3 Boiling Point : -
Linear Structure Formula :NCC6H4NHNH3Cl InChI Key :UXDLLFIRCVPPQP-UHFFFAOYSA-N
M.W : 169.61 Pubchem ID :16212962
Synonyms :
4-Cyanophenylhydrazine hydrochloride
Chemical Name :4-Hydrazinylbenzonitrile hydrochloride

Calculated chemistry of [ 2863-98-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 45.33
TPSA : 61.84 ?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 : Yes
Log Kp (skin permeation) : -6.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.22
Log Po/w (WLOGP) : 1.46
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : 0.3
Consensus Log Po/w : 0.81

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.0
Solubility : 1.7 mg/ml ; 0.0101 mol/l
Class : Very soluble
Log S (Ali) : -2.12
Solubility : 1.3 mg/ml ; 0.00766 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.14
Solubility : 1.22 mg/ml ; 0.00721 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.63

Safety of [ 2863-98-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 2863-98-1 ]

* 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 [ 2863-98-1 ]

[ 2863-98-1 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 29882-07-3 ]
  • [ 2863-98-1 ]
  • [ 46276-24-8 ]
  • 2
  • [ 2863-98-1 ]
  • [ 104618-32-8 ]
  • [ 147009-18-5 ]
YieldReaction ConditionsOperation in experiment
With sodium acetate; In acetic acid; 4-Cyanophenyl hydrazine hydrochloride (4.41 g, 0.026 mole) was dissolved in acetic acid (100 ml) and sodium acetate (2 g) was added. 4-Phthalimido cyclohexanone (6.4 g, 0.026 mole) was added and the mixture heated under reflux overnight. The solvent was removed in vacuo and the residue triturated with methanol to give 3-phthalimido-6-cyano-1,2,3,4-tetrahydrocarbazole as a beige solid, (5.3 g).
  • 3
  • [ 29882-07-3 ]
  • [ 2863-98-1 ]
  • 3-(2-aminoethyl)-5-cyano-1H-indole hydrochloride [ No CAS ]
  • 4
  • [ 720-94-5 ]
  • [ 2863-98-1 ]
  • 4-[5-(4-Methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% In ethanol; for 7h;Reflux; General procedure: To a warm ethanolic solution (10mL) of 4-hydrazinylbenzonitrile hydrochloride 4 (350mg, 2.0mmol) was added appropriate trifluoromethyl-beta-diketone 5a?5i (2.0mmol) while stirring and the contents were refluxed for 7h. The progress of the reaction was monitored by TLC. When the reaction was completed, excess solvent was evaporated to reduce the volume to one half whereupon reaction mixture was allowed to cool to 20?25°C and the solid thus obtained was filtered to obtain 2a?2i (85?93percent).
  • 5
  • [ 34846-90-7 ]
  • [ 2863-98-1 ]
  • 1-(4-cyanophenyl)-5-hydroxypyrazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
64.2% In methanol; for 6h;Reflux; 1.70 g (10 mmol) of 4-cyanophenylhydrazine hydrochloride, 1.16 g (10 mmol) of methoxypropan-2-ol were added to a three-necked reaction flaskMethylene chloride, 10 mL of methanol. The temperature of the reaction mixture was raised to reflux for about 6 hours. The reaction solution was quantitated by liquid chromatography, and 1- (4-cyanoPhenyl) -5-hydroxypyrazole Yield 64.2percent
  • 6
  • [ 2863-98-1 ]
  • [ 622-88-8 ]
  • [ 1591-30-6 ]
  • [ 57774-35-3 ]
  • [ 92-86-4 ]
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