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[ CAS No. 2924-09-6 ] {[proInfo.proName]}

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Chemical Structure| 2924-09-6
Chemical Structure| 2924-09-6
Structure of 2924-09-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2924-09-6 ]

CAS No. :2924-09-6 MDL No. :MFCD03094181
Formula : C6H5BrFN Boiling Point : No data available
Linear Structure Formula :- InChI Key :ADWKOCXRCRSMLQ-UHFFFAOYSA-N
M.W : 190.01 Pubchem ID :2769407
Synonyms :

Calculated chemistry of [ 2924-09-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.5
TPSA : 26.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.73
Log Po/w (XLOGP3) : 2.13
Log Po/w (WLOGP) : 2.6
Log Po/w (MLOGP) : 2.67
Log Po/w (SILICOS-IT) : 2.25
Consensus Log Po/w : 2.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.85
Solubility : 0.266 mg/ml ; 0.0014 mol/l
Class : Soluble
Log S (Ali) : -2.31
Solubility : 0.935 mg/ml ; 0.00492 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.17
Solubility : 0.128 mg/ml ; 0.000673 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 2924-09-6 ]

Signal Word:Warning Class:
Precautionary Statements:P273-P305+P351+P338 UN#:
Hazard Statements:H302-H319-H412 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2924-09-6 ]

* 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.

  • Upstream synthesis route of [ 2924-09-6 ]
  • Downstream synthetic route of [ 2924-09-6 ]

[ 2924-09-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 2924-09-6 ]
  • [ 140-89-6 ]
  • [ 71216-20-1 ]
YieldReaction ConditionsOperation in experiment
95% at 140℃; for 2 h; Step A: 5-Bromobenzothiazole-2-thiol; To a solution of 5-bromo-2-fluorobenzenamine (200 mg, 1.28 mmol) in N-methyl-2- pyrrolidine (1.5 mL) was added potassium o-ethyl carbonodithioate (410 mg, 2.56 mmol). The mixture was heated at 140 0C for 2 h. The reaction mixture was poured into a large amount of water, acidified with concentrated hydrochloric acid, and filtered to give 5-bromo- benzothiazole-2-thiol 300 mg (95 percent).
Reference: [1] Patent: WO2007/110364, 2007, A1, . Location in patent: Page/Page column 57
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