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[ CAS No. 5900-13-0 ] {[proInfo.proName]}

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Chemical Structure| 5900-13-0
Chemical Structure| 5900-13-0
Structure of 5900-13-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5900-13-0 ]

CAS No. :5900-13-0 MDL No. :MFCD08275726
Formula : C5H6BrN3O Boiling Point : -
Linear Structure Formula :- InChI Key :QDFJJHGAODFQMN-UHFFFAOYSA-N
M.W : 204.03 Pubchem ID :11344724
Synonyms :

Calculated chemistry of [ 5900-13-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.63
TPSA : 61.03 ?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) : -7.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 0.76
Log Po/w (WLOGP) : 0.84
Log Po/w (MLOGP) : -0.07
Log Po/w (SILICOS-IT) : 0.89
Consensus Log Po/w : 0.82

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.96
Solubility : 2.23 mg/ml ; 0.0109 mol/l
Class : Very soluble
Log S (Ali) : -1.62
Solubility : 4.88 mg/ml ; 0.0239 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.28
Solubility : 1.07 mg/ml ; 0.00526 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.65

Safety of [ 5900-13-0 ]

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

Application In Synthesis of [ 5900-13-0 ]

* 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 [ 5900-13-0 ]

[ 5900-13-0 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 4774-10-1 ]
  • [ 5900-13-0 ]
  • 3
  • [ 5900-13-0 ]
  • [ 163295-70-3 ]
  • N-(5-bromo-3-methoxypyrazin-2-yl)-1-(3,5-dichlorophenyl)methanesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
54% With dmap; at 20℃; for 3h;Inert atmosphere; To a stirring solution of 5-bromo-3-methoxypyrazin-2-amine (1.50 g, 7.35 mmol) in pyridine (15 mL), DMAP (15 mg, 0.12 mmol) and <strong>[163295-70-3](3,5-dichlorophenyl)methanesulfonyl chloride</strong> (1.91 g, 7.34 mmol) was added. The reaction was left stirring at room temperature under nitrogen for 2 hrs. A further addition of <strong>[163295-70-3](3,5-dichlorophenyl)methanesulfonyl chloride</strong> (0.20 g, 0.77 mmol) was added to the reaction mixture which was then left stirring for 1 hr at room temperature. The reaction mixture was concentrated in vacuo resulting in a viscous orange mixture which was then diluted with EtOAc (100 mL), washed with water (2 x 80 mL), the organic layer was dried over Na2S04 and concentrated in vacuo to afford an orange solid. This was dissolved in EtOAc (30 mL) and acidified with HCl (2M, 20 mL) which resulted in the precipitation of the title compound as a white solid . The organic and aqueous layer were subsequently separated, the organic layer was washed with water (3 x 30 mL), dried over Na2S04 and concentrated in vacuo to afford a second crop of the title compound as an orange solid (combined yield 1.73g, 54%); H NMR (500 MHz, DMSO) δ 3.93 (s, 3H), 4.88 (s, 2H), 7.36 (d, 2H), 7.63 (m, 1H), 8.12 (s, 1H), 10.80 (s, 1H).
  • 4
  • [ 5900-13-0 ]
  • [ 163295-70-3 ]
  • N-(5-cyano-3-methoxypyrazin-2-yl)-1-(3,5-dichlorophenyl)methanesulfonamide [ No CAS ]
  • 5
  • [ 5900-13-0 ]
  • [ 4774-10-1 ]
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