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[ CAS No. 26032-72-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 26032-72-4
Chemical Structure| 26032-72-4
Structure of 26032-72-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 26032-72-4 ]

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Product Details of [ 26032-72-4 ]

CAS No. :26032-72-4 MDL No. :MFCD00234591
Formula : C10H6Cl2N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VRNSMZDBMUSIFT-UHFFFAOYSA-N
M.W : 225.07 Pubchem ID :241554
Synonyms :

Calculated chemistry of [ 26032-72-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 57.49
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.98 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.5
Log Po/w (XLOGP3) : 3.79
Log Po/w (WLOGP) : 3.45
Log Po/w (MLOGP) : 2.43
Log Po/w (SILICOS-IT) : 3.73
Consensus Log Po/w : 3.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.19
Solubility : 0.0145 mg/ml ; 0.0000644 mol/l
Class : Moderately soluble
Log S (Ali) : -4.03
Solubility : 0.0212 mg/ml ; 0.0000943 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.41
Solubility : 0.000878 mg/ml ; 0.0000039 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.88

Safety of [ 26032-72-4 ]

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

Application In Synthesis of [ 26032-72-4 ]

* 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 [ 26032-72-4 ]

[ 26032-72-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 26032-72-4 ]
  • [ 22237-13-4 ]
  • 2-chloro-4-(4-ethoxyphenyl)-6-phenylpyrimidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With palladium diacetate; sodium carbonate; triphenylphosphine; In 1,2-dimethoxyethane; water; at 85℃; for 24h;Inert atmosphere; General procedure: To a solution of 2,4,6-trichloropyrimidine (1.0 eq) in degassed DME (9 mL/mmol)arylboronic acid (1.0 eq, or 2 eq for symmetrical analogues), a solution of Na2CO3(3.1 eq) in degassed water (1 mL/mmol), PPh3 (3.5 mol%) and Pd(OAc)2(1.3 mol%) were added under an argon atmosphere. The reaction mixture wasrefluxed at 85 C for 24 h and then concentrated in vacuo. The residue waspartitioned between water and CH2Cl2 and extracted. Theorganic layers were washed with brine, dried (Na2SO4) andconcentrated in vacuo to givethe crude product.
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