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[ CAS No. 192441-08-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 192441-08-0
Chemical Structure| 192441-08-0
Structure of 192441-08-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 192441-08-0 ]

CAS No. :192441-08-0 MDL No. :MFCD23703756
Formula : C10H8BrN5OS Boiling Point : -
Linear Structure Formula :- InChI Key :JUJPKFNFCWJBCX-UHFFFAOYSA-N
M.W : 326.17 Pubchem ID :3025944
Synonyms :
PaTrin-2
Chemical Name :6-((4-Bromothiophen-2-yl)methoxy)-9H-purin-2-amine

Calculated chemistry of [ 192441-08-0 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 14
Fraction Csp3 : 0.1
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 72.64
TPSA : 117.95 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 1.96
Log Po/w (WLOGP) : 2.19
Log Po/w (MLOGP) : 0.82
Log Po/w (SILICOS-IT) : 2.97
Consensus Log Po/w : 1.97

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.47
Solubility : 0.109 mg/ml ; 0.000335 mol/l
Class : Soluble
Log S (Ali) : -4.06
Solubility : 0.0283 mg/ml ; 0.0000867 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.57
Solubility : 0.00884 mg/ml ; 0.0000271 mol/l
Class : Moderately soluble

Medicinal Chemistry

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

Safety of [ 192441-08-0 ]

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

Application In Synthesis of [ 192441-08-0 ]

* 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 [ 192441-08-0 ]

[ 192441-08-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 79757-77-0 ]
  • [ 34798-95-3 ]
  • [ 192441-08-0 ]
YieldReaction ConditionsOperation in experiment
69% With sodium hydride; In N,N-dimethyl-formamide; at 30℃; for 2h; 4-Bromothienylmethanol (1.32 g, 6.9 mmol) was weighed into a 100 mL round bottom flask,18 mL of N, N-dimethylformamide was added,To the reaction solution was added sodium hydride (0.110 g, 4.6 mmol) and 2-aminopurine-6-trimethylammonium chloride (0.525 g, 2.3 mmol)30 , stirring reaction 2h.After the reaction,Adding ethyl acetate and water in accordance with the volume of 1: 1 composition of the mixture for extraction,After the organic phase was washed with saturated ammonium chloride solution,Dried over anhydrous sodium sulphate,30 vacuum distillation,The resulting crude product was dissolved in methanol,Filter to remove impurities,Recrystallization gave (6- (4-bromothiophenoxy) -9-hydrogen-purin-2) amine (0.517 g, 1.59 mmol) in 69% yield.
Same Skeleton Products
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