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[ CAS No. 949922-61-6 ] {[proInfo.proName]}

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Chemical Structure| 949922-61-6
Chemical Structure| 949922-61-6
Structure of 949922-61-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 949922-61-6 ]

CAS No. :949922-61-6 MDL No. :MFCD09701262
Formula : C11H16BrN3O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YTGNTPFZMKDHEY-UHFFFAOYSA-N
M.W : 302.17 Pubchem ID :37819064
Synonyms :
Chemical Name :tert-Butyl 3-bromo-5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate

Calculated chemistry of [ 949922-61-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.64
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 71.41
TPSA : 47.36 ?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) : -7.11 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.79
Log Po/w (XLOGP3) : 1.46
Log Po/w (WLOGP) : 1.86
Log Po/w (MLOGP) : 1.17
Log Po/w (SILICOS-IT) : 1.04
Consensus Log Po/w : 1.67

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 : 0.672 mg/ml ; 0.00222 mol/l
Class : Soluble
Log S (Ali) : -2.06
Solubility : 2.63 mg/ml ; 0.00869 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.32
Solubility : 1.46 mg/ml ; 0.00483 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.86

Safety of [ 949922-61-6 ]

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 [ 949922-61-6 ]

* 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 [ 949922-61-6 ]

[ 949922-61-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 345311-03-7 ]
  • [ 949922-61-6 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; In tetrachloromethane; for 0.5h;Reflux; General Process for the Preparation of Compound E-In-3 from E-In-2: [00128] A round bottom flask was charged with E-In-2 (1 eq.), CCl4 and N- bromosuccinimide (1 eq.). The solution was refluxed for 30 minutes then allowed to cool. The CCl4 solution was decanted off a brown solid and evaporated. The residue was purified by trituration, or recrystallization, or silica gel column chromatography, or Shimadzu automated preparative HPLC system, to afford E-In-3.
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