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[ CAS No. 1161763-15-0 ] {[proInfo.proName]}

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Chemical Structure| 1161763-15-0
Chemical Structure| 1161763-15-0
Structure of 1161763-15-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1161763-15-0 ]

CAS No. :1161763-15-0 MDL No. :MFCD12923091
Formula : C5H6BrN3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AEWWKIWMCYZMJY-UHFFFAOYSA-N
M.W : 188.03 Pubchem ID :56965719
Synonyms :

Calculated chemistry of [ 1161763-15-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.1
TPSA : 51.8 ?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) : -6.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.8
Log Po/w (XLOGP3) : 1.28
Log Po/w (WLOGP) : 1.14
Log Po/w (MLOGP) : 0.51
Log Po/w (SILICOS-IT) : 1.34
Consensus Log Po/w : 1.22

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.31
Solubility : 0.931 mg/ml ; 0.00495 mol/l
Class : Soluble
Log S (Ali) : -1.97
Solubility : 2.03 mg/ml ; 0.0108 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.54
Solubility : 0.549 mg/ml ; 0.00292 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.17

Safety of [ 1161763-15-0 ]

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

Application In Synthesis of [ 1161763-15-0 ]

* 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 [ 1161763-15-0 ]

[ 1161763-15-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1161763-15-0 ]
  • [ 72605-86-8 ]
  • [ 1245157-45-2 ]
YieldReaction ConditionsOperation in experiment
78.4% 60% sodium hydride (12.0 g, 0.30 mol) was suspended in THF (300 mL) and cooled down to 0 C. 4-amino-6-bromo-2-methylpyrimidine (Compound 9) (18.7 g, 0.1 mol) was then added in batches and stirred for 30 min. After <strong>[72605-86-8]methyl 2-chlorothiazole-5-formate</strong> (Compound 10) (17.7 g, 0.1 mol) was added in batches, the reactants were heated and reacted by refluxing for 4 h, and then cooled down to room temperature for reaction overnight. When controlling the temperature between 0 C. and 5 C., hydrochloric acid (2N) was added for neutralization reaction. After adding keep heat and stirred to grow grains for 1 h. Filtrate and wash the cake with water, and then dry to give target Compound 11 (25.8 g, yield is 78.4%).[0177]Element analysis: C10H9BrN4O2S, Calculated: C, 36.49; H, 2.76; N, 17.02. Found: C, 36.51; H, 2.77; N, 16.99.[0178]1H-NMR (500 MHz, DMSO-d6): delta(ppm) 2.580 (s, 3H), 3.820 (s, 3H), 6.960 (S, 1H), 8.160 (s, 1H), 12.376 (s, 1H) (which disappeared after exchanging D2O)[0179]13C-NMR (500 MHz, DMSO-d6): delta(ppm) 25.700, 52.800, 104.161, 121.662, 146.010, 157.910, 159.124, 162.412, 162.949, 167.871.
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