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[ CAS No. 2905-24-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 2905-24-0
Chemical Structure| 2905-24-0
Structure of 2905-24-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2905-24-0 ]

CAS No. :2905-24-0 MDL No. :MFCD00052313
Formula : C6H4BrClO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :PJGOLCXVWIYXRQ-UHFFFAOYSA-N
M.W : 255.52 Pubchem ID :17943
Synonyms :

Calculated chemistry of [ 2905-24-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.23
TPSA : 42.52 ?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) : -5.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 2.81
Log Po/w (WLOGP) : 3.46
Log Po/w (MLOGP) : 2.28
Log Po/w (SILICOS-IT) : 2.02
Consensus Log Po/w : 2.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.53
Solubility : 0.075 mg/ml ; 0.000294 mol/l
Class : Soluble
Log S (Ali) : -3.36
Solubility : 0.112 mg/ml ; 0.000436 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.79
Solubility : 0.041 mg/ml ; 0.00016 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.94

Safety of [ 2905-24-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2905-24-0 ]

* 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 [ 2905-24-0 ]

[ 2905-24-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2905-24-0 ]
  • [ 50413-30-4 ]
  • [ 1197897-37-2 ]
  • 2
  • [ 2905-24-0 ]
  • [ 15861-23-1 ]
  • C15H11BrN2O2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% With triethylamine; In dichloromethane; at 20℃; The 5 - cyano - indoline (1.00 g, 6. 94 mmol) and TEA (2.88 ml, 20.8 mmol) dissolved in DCM (30 ml) in, adding 3 - bromo - benzenesulfonyl chloride (1.95 g, 7.63 mmol) At room temperature overnight and for. Water quenching reaction, divide the DCM layer, for extracting the alternating layer twice twice DCM, the combined DCM layer turns on lathe does after drying, a yellow solid intermediate 1 a (2.26 g, yield: 90%) .
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