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[ CAS No. 3034-55-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3034-55-7
Chemical Structure| 3034-55-7
Structure of 3034-55-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 3034-55-7 ]

CAS No. :3034-55-7 MDL No. :MFCD07787394
Formula : C3H2BrNS Boiling Point : No data available
Linear Structure Formula :- InChI Key :DWUPYMSVAPQXMS-UHFFFAOYSA-N
M.W : 164.02 Pubchem ID :546059
Synonyms :

Calculated chemistry of [ 3034-55-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 29.81
TPSA : 41.13 ?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) : -5.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.54
Log Po/w (XLOGP3) : 1.98
Log Po/w (WLOGP) : 1.91
Log Po/w (MLOGP) : 0.53
Log Po/w (SILICOS-IT) : 3.07
Consensus Log Po/w : 1.81

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.72
Solubility : 0.312 mg/ml ; 0.0019 mol/l
Class : Soluble
Log S (Ali) : -2.47
Solubility : 0.556 mg/ml ; 0.00339 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.14
Solubility : 1.2 mg/ml ; 0.00729 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.27

Safety of [ 3034-55-7 ]

Signal Word:Danger Class:
Precautionary Statements:P210-P261-P264-P270-P271-P272-P280-P301+P312+P330-P302+P352-P304+P340+P312-P305+P351+P338+P310-P333+P313-P370+P378-P403+P233-P403+P235-P405-P501 UN#:
Hazard Statements:H302-H315-H317-H318-H335-H227 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 3034-55-7 ]

* 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 [ 3034-55-7 ]

[ 3034-55-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3034-55-7 ]
  • [ 489446-42-6 ]
  • tert-butyl 4-(thiazol-5-yl)benzylcarbamate [ No CAS ]
  • 2
  • [ 3034-55-7 ]
  • [ 452972-11-1 ]
  • 2-chloro-3-(thiazol-5-yl)-pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In 1,4-dioxane; water; at 120℃; for 0.25h;Microwave irradiation; Svnthesis 32 2-Chlor -3-thiazol-5-yl-pyridine To a degassed suspension of 5-bromothiazole (3 mmol, 0.5 g) and 2-chloro-3-(4, 4,5,5- tetramethyl-[1 ,3,2]dioxaborolan-2-yl)-pyridine (3 mmol, 0.73 g) in 1 ,4-dioxane (14 mL) water (6 mL) was added potassium carbonate (9 mmol, 1.25 g) and bis(triphenylphenylphospine) palladium (II) dichloride (0.15 mmol, 0.10 g). The mixture was heated in a microwave reactor at 120 C for 15 minutes. The mixture was purified by flash chromatography using a gradient elution of 0-100% ethyl acetate/cyclohexane. The solvent was removed by evaporation under reduced pressure to yield the title compound as a low-melting point colourless solid. Yield: 0.42 g, 72%. LCMS, analytical method 1 , TR= 3.37 mins, 95%, M+H=197. H NMR (300 MHz, CDCIs) delta: 8.92 (1 H, s), 8.42 (1 H, d), 8.15 (1 H, s), 7.85 (1 H, d), 7.35 (1 H, m).
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