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[ CAS No. 98198-48-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 98198-48-2
Chemical Structure| 98198-48-2
Structure of 98198-48-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 98198-48-2 ]

CAS No. :98198-48-2 MDL No. :MFCD03427660
Formula : C6H7BrN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JDNCMHOKWINDKI-UHFFFAOYSA-N
M.W : 187.04 Pubchem ID :817695
Synonyms :

Calculated chemistry of [ 98198-48-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.31
TPSA : 38.91 ?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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.58
Log Po/w (XLOGP3) : 1.56
Log Po/w (WLOGP) : 1.74
Log Po/w (MLOGP) : 1.33
Log Po/w (SILICOS-IT) : 1.78
Consensus Log Po/w : 1.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.48
Solubility : 0.625 mg/ml ; 0.00334 mol/l
Class : Soluble
Log S (Ali) : -1.99
Solubility : 1.93 mg/ml ; 0.0103 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.232 mg/ml ; 0.00124 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.6

Safety of [ 98198-48-2 ]

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

Application In Synthesis of [ 98198-48-2 ]

* 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 [ 98198-48-2 ]

[ 98198-48-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 695-34-1 ]
  • [ 98198-48-2 ]
  • [ 3430-29-3 ]
  • 3
  • [ 98198-48-2 ]
  • [ 164513-38-6 ]
YieldReaction ConditionsOperation in experiment
31% With sodium nitrite; In sulfuric acid; water; a 3-Bromo-6-hydroxy-4-methyl pyridine Sodium nitrite (5.44 g, 78.8 mmol) in water (14 ml) was added dropwise to 2-amino-5-bromo-4-methylpyridine (12.83 g, 68.6 mmol) in sulphuric acid (20%) (69 ml) at 0-5 C. After 1 h at 0 C. the solution was heated to reflux for 1 h. The solution was basified to pH 10 with sodium hydroxide solution (40%) and cooled to 5 C. and the precipitated product separated by filtration. Recrystallisation from ethanol gave the title compound (5.97 g, 31%) as white needles (m.p.200-201 C.); δH (D6 -DMSO) 2.17 (3H, s, CH3), 6.40 (1H, s, 3-H), 7.76 (1H, s, 6-H), 11.58 (1H, s, NH): m/z (E.I.) 189 (M+, 100%), 187 (M+, 97%); (Found: M+, 186.9634. C6 H6 NOBr requires M, 186.9633).
  • 4
  • [ 98198-48-2 ]
  • [ 108-24-7 ]
  • [ 142404-82-8 ]
YieldReaction ConditionsOperation in experiment
5-bromo-4-methylpyridin-2-amine (0.578 mmol) was dissolved in acetic anhydride (5.78 mmol) and heated at 1 10 C for 30 minutes. The reaction was quenched with ice. The aqueous reaction mixture neutralized with sodium hydroxide solution was extracted with ethyl acetate. The ethyl acetate layer was separated and dried over sodium sulfate. The organic layer was evaporated to dryness. The crude material was purified (silica column, MeOH/CHCL). 1HNMR (300MHz, DMSO-d6): 10.53 (s, 1H), 8.34 (s, 1H), 8.06 (s, 1H), 2.30 (s, 3H), 2.05 (s, 3H); MS (m/z): 231 (M+2)+.
  • 5
  • [ 98198-48-2 ]
  • [ 1150617-52-9 ]
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