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[ CAS No. 3034-48-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3034-48-8
Chemical Structure| 3034-48-8
Structure of 3034-48-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 3034-48-8 ]

CAS No. :3034-48-8 MDL No. :MFCD00005317
Formula : C3HBrN2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :ANIJFZVZXZQFDH-UHFFFAOYSA-N
M.W : 209.02 Pubchem ID :18211
Synonyms :

Calculated chemistry of [ 3034-48-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.64
TPSA : 86.95 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.21
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 1.81
Log Po/w (MLOGP) : -0.67
Log Po/w (SILICOS-IT) : 1.02
Consensus Log Po/w : 1.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.87
Solubility : 0.284 mg/ml ; 0.00136 mol/l
Class : Soluble
Log S (Ali) : -3.66
Solubility : 0.0457 mg/ml ; 0.000219 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.53
Solubility : 6.11 mg/ml ; 0.0292 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.99

Safety of [ 3034-48-8 ]

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

Application In Synthesis of [ 3034-48-8 ]

* 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 [ 3034-48-8 ]

[ 3034-48-8 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 121-66-4 ]
  • [ 3034-48-8 ]
YieldReaction ConditionsOperation in experiment
With sodium nitrite; Example 12 3-[(5-nitrothiazol-2-yl)mercapto]-5-phenyl-1,2,4-triazole (SU4390) (Compound 7) The key starting material 2-bromo-5-nitrothiazole was prepared by treating 2-amino-5-nitrothiazole (Aldrich) with sodium nitrite and hydrogen bromide (Fr. Demande 2,015,434, 1970).
With sodium nitrite; Example 1 3-[(5-nitrothiazol-2-yl)mercapto]-5-phenyl-1,2,4-triazole (Compound 1) The starting material 2-bromo-5-nitrothiazole was prepared by treating 2-amino-5-nitrothiazole (Aldrich) with sodium nitrite and hydrogen bromide (Fr. Demande 2,015,434, 1970).
With sodium nitrite; Example 1 3-[(5-nitrothiazol-2-yl)mercapto]-5-phenyl-1,2,4-triazole (Compound 7) The starting material 2-bromo-5-nitrothiazole was prepared by treating 2-amino-5-nitrothiazole (Aldrich) with sodium nitrite and hydrogen bromide (Fr. Demande 2,015,434, 1970).
  • 2
  • [ 3034-48-8 ]
  • [ 14527-46-9 ]
  • 3
  • [ 3034-48-8 ]
  • [ 3034-49-9 ]
  • 6
  • [ 28118-54-9 ]
  • [ 3034-48-8 ]
  • [ 61-57-4 ]
  • 7
  • [ 110-85-0 ]
  • [ 3034-48-8 ]
  • [ 17832-56-3 ]
  • 8
  • [ 1121-92-2 ]
  • [ 3034-48-8 ]
  • [ 21166-10-9 ]
  • 9
  • [ 20112-79-2 ]
  • [ 3034-48-8 ]
  • [ 37422-15-4 ]
  • 10
  • [ 6602-28-4 ]
  • [ 3034-48-8 ]
  • 3-(5-nitro-thiazol-2-yloxy)-pyridine 1-oxide [ No CAS ]
  • 11
  • [ 6320-03-2 ]
  • [ 3034-48-8 ]
  • [ 53316-68-0 ]
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