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[ CAS No. 57473-32-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 57473-32-2
Chemical Structure| 57473-32-2
Structure of 57473-32-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 57473-32-2 ]

CAS No. :57473-32-2 MDL No. :MFCD06858696
Formula : C6H3Cl2N3 Boiling Point : -
Linear Structure Formula :- InChI Key :WMHORUUVAKBDSV-UHFFFAOYSA-N
M.W : 188.01 Pubchem ID :23125107
Synonyms :

Calculated chemistry of [ 57473-32-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.01
TPSA : 30.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 3.04
Log Po/w (WLOGP) : 2.04
Log Po/w (MLOGP) : 1.38
Log Po/w (SILICOS-IT) : 1.77
Consensus Log Po/w : 1.94

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.53
Solubility : 0.056 mg/ml ; 0.000298 mol/l
Class : Soluble
Log S (Ali) : -3.34
Solubility : 0.086 mg/ml ; 0.000457 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.95
Solubility : 0.212 mg/ml ; 0.00113 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.73

Safety of [ 57473-32-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 57473-32-2 ]

* 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 [ 57473-32-2 ]

[ 57473-32-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 57473-32-2 ]
  • [ 53332-78-8 ]
  • 7-chloro-N-(thiazol-2-ylmethyl)imidazo[1,2-a]pyrimidin-5-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% With triethylamine; In 1,4-dioxane; at 70℃;Inert atmosphere; General procedure: Example 8. General Procedure H A mixture of the desired chloroimidazopyrimidines i-H (1 equiv), desired aminomethyl heterocycle or benzylamine ii-H (1.2 equiv), and triethylamine (NEt3) (1.5-3.5 equiv) in 1,4-dioxane (~0.1 M) was stirred at 70 C until the reaction was complete by LC-MS and/or TLC analysis. The crude reaction mixture was directly purified by silica gel chromatography (typical eluents included, for example, a mixture of hexanes and EtOAc, or a mixture of CH2Cl2 and MeOH, or an 80:18:2 mixture of CH2Cl2/CH3OH/concentrated NH4OH) to afford the desired product iii-H. The product structures prepared according to General Procedure H were confirmed by 1H NMR and/or by mass analysis.
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