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[ CAS No. 70260-16-1 ] {[proInfo.proName]}

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Chemical Structure| 70260-16-1
Chemical Structure| 70260-16-1
Structure of 70260-16-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 70260-16-1 ]

CAS No. :70260-16-1 MDL No. :MFCD09025881
Formula : C5H5BrOS Boiling Point : -
Linear Structure Formula :- InChI Key :BOJYRNFSHPAZBL-UHFFFAOYSA-N
M.W : 193.06 Pubchem ID :12479010
Synonyms :

Calculated chemistry of [ 70260-16-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.15
TPSA : 48.47 ?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) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.77
Log Po/w (XLOGP3) : 1.74
Log Po/w (WLOGP) : 1.85
Log Po/w (MLOGP) : 1.29
Log Po/w (SILICOS-IT) : 3.07
Consensus Log Po/w : 1.94

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.53
Solubility : 0.57 mg/ml ; 0.00295 mol/l
Class : Soluble
Log S (Ali) : -2.37
Solubility : 0.815 mg/ml ; 0.00422 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.35
Solubility : 0.86 mg/ml ; 0.00446 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.48

Safety of [ 70260-16-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 70260-16-1 ]

* 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 [ 70260-16-1 ]

[ 70260-16-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 70260-16-1 ]
  • [ 1860-99-7 ]
YieldReaction ConditionsOperation in experiment
83% With Dess-Martin periodane In tetrahydrofuran at 0℃; for 3 h; To a solution of (2-bromothiophen-3-yl)methanol (5 g, 26.3 mmol) in THF (60 mL) at 0 °C was added Dess-Martin periodinane (13.4 g, 31.6 mmol) in portions. After stirring at 0 °C for 3 h, water and Na2S03 were added. The mixture was extracted with DCM, and the combined organic layers were washed with brine and dried over anhydrous Na2S04. After filtration and concentration, the crude product was purified by column chromatography to give the title compound (4.1 g, 83percent).
Reference: [1] Patent: WO2011/69063, 2011, A2, . Location in patent: Page/Page column 95
[2] Patent: US5840917, 1998, A,
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