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[ CAS No. 41965-95-1 ] {[proInfo.proName]}

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Chemical Structure| 41965-95-1
Chemical Structure| 41965-95-1
Structure of 41965-95-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 41965-95-1 ]

CAS No. :41965-95-1 MDL No. :MFCD01211460
Formula : C8H11Cl2NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :IKWWOZCEHOYKAO-UHFFFAOYSA-N
M.W : 208.09 Pubchem ID :2764287
Synonyms :

Calculated chemistry of [ 41965-95-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 52.58
TPSA : 35.25 ?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 : No
Log Kp (skin permeation) : -6.13 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.03
Log Po/w (WLOGP) : 2.46
Log Po/w (MLOGP) : 2.1
Log Po/w (SILICOS-IT) : 2.06
Consensus Log Po/w : 1.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.65
Solubility : 0.469 mg/ml ; 0.00225 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.832 mg/ml ; 0.004 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.18
Solubility : 0.137 mg/ml ; 0.000658 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.32

Safety of [ 41965-95-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P280-P301+P310+P330-P302+P352-P305+P351+P338+P310 UN#:2811
Hazard Statements:H301-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 41965-95-1 ]

* 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 [ 41965-95-1 ]

[ 41965-95-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 178308-61-7 ]
  • [ 41965-95-1 ]
  • [ 178308-63-9 ]
  • 4-Chloro-1-(3-chloro-4-methoxybenzyl)amino-6-cyanophthalazine [ No CAS ]
  • 2
  • [ 4903-09-7 ]
  • aqueous sodium cyanacetate [ No CAS ]
  • [ 41965-95-1 ]
  • 3
  • [ 41965-95-1 ]
  • [ 330785-84-7 ]
  • 4
  • [ 1246834-64-9 ]
  • [ 23356-96-9 ]
  • [ 41965-95-1 ]
  • [ 2972-52-3 ]
  • [ 330784-47-9 ]
YieldReaction ConditionsOperation in experiment
64% A solution of 2,4-dichloro-5-pyrimidinecarbonyl chloride (0.6 g, 2.8 mmol) in dichloromethane (8 ml) was added to a 50 ml three-necked flask and cooled in an ice bath. The 2-aminomethylpyrimidine acetate (0.48 g, 2.8 mmol) and triethylamine (2.8 mmol) were first dissolved in dichloromethane,And then dropwise dropwise into the reaction solution. Plus finished, the reaction 1 hour,A mixture of 3-chloro-4-methoxybenzylamine hydrochloride (0.59 g, 2.8 mmol) and triethylamine (0.29 g, 2.8 mmol) was added dropwise to the above reaction solution, 2 hours,To the reaction solution was added L-proline alcohol (0.43 g, 4.3 mmol), and the reaction was carried out overnight at room temperature.The reaction solution was poured into ice water, quenched and extracted twice with methylene chloride. The organic phase was combined and washed twice with water,Dried over anhydrous sodium sulfate and concentrated to give the crude product which was purified by column chromatography to give 0.9 g of white solid, and the yield was 64%.
  • 5
  • [ 102151-33-7 ]
  • [ 41965-95-1 ]
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