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[ CAS No. 4549-32-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4549-32-0
Chemical Structure| 4549-32-0
Structure of 4549-32-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4549-32-0 ]

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Product Details of [ 4549-32-0 ]

CAS No. :4549-32-0 MDL No. :MFCD00000277
Formula : C8H16Br2 Boiling Point : -
Linear Structure Formula :Br(CH2)8Br InChI Key :DKEGCUDAFWNSSO-UHFFFAOYSA-N
M.W : 272.02 Pubchem ID :78310
Synonyms :

Calculated chemistry of [ 4549-32-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 7
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 56.31
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
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) : -4.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.2
Log Po/w (XLOGP3) : 4.26
Log Po/w (WLOGP) : 4.12
Log Po/w (MLOGP) : 4.2
Log Po/w (SILICOS-IT) : 3.93
Consensus Log Po/w : 3.94

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.75
Solubility : 0.0486 mg/ml ; 0.000179 mol/l
Class : Soluble
Log S (Ali) : -3.97
Solubility : 0.029 mg/ml ; 0.000107 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.82
Solubility : 0.0041 mg/ml ; 0.0000151 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.36

Safety of [ 4549-32-0 ]

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 [ 4549-32-0 ]

* 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 [ 4549-32-0 ]

[ 4549-32-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 4549-32-0 ]
  • [ 42726-73-8 ]
  • 2-(8-Bromo-octyl)-malonic acid tert-butyl ester methyl ester [ No CAS ]
  • 2
  • [ 4549-32-0 ]
  • [ 42019-78-3 ]
  • [ 1010071-49-4 ]
  • 3
  • [ 33893-89-9 ]
  • [ 4549-32-0 ]
  • [ 1443682-07-2 ]
  • [ 1443682-08-3 ]
YieldReaction ConditionsOperation in experiment
17%; 19% General procedure: To L1 (2.00 g, 13.6 mmol) dissolved in acetonitrile (60 mL) was added potassium carbonate (18.8 g, 136 mmol). The resulting solution was heated at reflux temperature for 30 min and to the hot solution was added 1,n-dibromoalkane (48.0 mmol, n=3, 4, 6 or 8). The reaction mixture was then stirred at reflux temperature for a further 24 . After cooling, the inorganic solids were removed by filtration and the solvent was removed under reduced pressure to afford an oil, which was purified by column chromatography on silica gel (initially at a ratio of petroleum ether:ethyl acetate 80:20, followed by the ratio of 60:40). This gave the products L2A-D and L3A-D.
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