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[ CAS No. 75833-38-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 75833-38-4
Chemical Structure| 75833-38-4
Structure of 75833-38-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 75833-38-4 ]

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Product Details of [ 75833-38-4 ]

CAS No. :75833-38-4 MDL No. :MFCD00234989
Formula : C5H2ClN3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HXVQPZSXXYOZMP-UHFFFAOYSA-N
M.W : 139.54 Pubchem ID :246647
Synonyms :

Calculated chemistry of [ 75833-38-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.76
TPSA : 49.57 ?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) : -6.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.25
Log Po/w (XLOGP3) : 1.22
Log Po/w (WLOGP) : 1.0
Log Po/w (MLOGP) : -0.43
Log Po/w (SILICOS-IT) : 1.54
Consensus Log Po/w : 0.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.97
Solubility : 1.51 mg/ml ; 0.0108 mol/l
Class : Very soluble
Log S (Ali) : -1.86
Solubility : 1.93 mg/ml ; 0.0139 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.33
Solubility : 0.657 mg/ml ; 0.00471 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.9

Safety of [ 75833-38-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 75833-38-4 ]

* 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 [ 75833-38-4 ]

[ 75833-38-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 114041-16-6 ]
  • [ 75833-38-4 ]
  • [ 1427927-36-3 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In acetonitrile; at 80℃; for 1h; Step 8) 2-c oropyrimidine derivative 11 (5.84 g, 42.0 mmol), DIEA (8 mL, 46 mmol) and isoindoline (7.52 mg, 42.0 mmol) were dissolved in Acetonitrile (100 mL) and the mixture was heated to 80C and stirred for 1 hour. The solvent was removed by concentration and water was added. The solid was collected with filtration, washed with water and dried under air. The crude 12 was used in the next step directly without further purification.
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