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[ CAS No. 18880-04-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 18880-04-1
Chemical Structure| 18880-04-1
Structure of 18880-04-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 18880-04-1 ]

CAS No. :18880-04-1 MDL No. :MFCD00041363
Formula : C7H5BrCl2 Boiling Point : -
Linear Structure Formula :- InChI Key :XLWSBDFQAJXCQX-UHFFFAOYSA-N
M.W : 239.92 Pubchem ID :639726
Synonyms :

Calculated chemistry of [ 18880-04-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.3
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.49
Log Po/w (XLOGP3) : 4.18
Log Po/w (WLOGP) : 3.74
Log Po/w (MLOGP) : 4.25
Log Po/w (SILICOS-IT) : 4.11
Consensus Log Po/w : 3.75

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.34
Solubility : 0.011 mg/ml ; 0.0000458 mol/l
Class : Moderately soluble
Log S (Ali) : -3.89
Solubility : 0.031 mg/ml ; 0.000129 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.89
Solubility : 0.00307 mg/ml ; 0.0000128 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.83

Safety of [ 18880-04-1 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2922
Hazard Statements:H301-H314-H413 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 18880-04-1 ]

* 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.

  • Downstream synthetic route of [ 18880-04-1 ]

[ 18880-04-1 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 16001-93-7 ]
  • [ 18880-04-1 ]
  • [2-(3,4-dichloro-phenyl)-1-(dimethoxy-phosphoryl)-ethyl]-phosphonic acid dimethyl ester [ No CAS ]
  • 2
  • [ 105-40-8 ]
  • [ 18880-04-1 ]
  • C11H13Cl2NO2 [ No CAS ]
  • 3
  • [ 37718-11-9 ]
  • [ 18880-04-1 ]
  • [ 1035224-45-3 ]
YieldReaction ConditionsOperation in experiment
91% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; To a solution of ethyl 1 H-pyrazole-4-carboxylate (0.475 g, 3.39 mmol) and potassium carbonate (0.56 g, 4.05 mmol) in DMF (20 ml.) was added dropwise 1 ,2-dichloro-4-(bromomethyl)benzene (0.98 g, 4.08 mmol) and the reaction mixture was stirred at room temperature overnight. After evaporation of the solvent under reduced pressure, the residue was diluted with water and extracted with DCM. The combined extracts were washed with brine, dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by flash column chromatography eluting with DCM/EtOAc: 92/8 to give the title compound as a white solid (0.92 g, 91percent). LC/MS: m/z 299 (M+H)+, Rt:3.44 min.
  • 4
  • [ 142273-20-9 ]
  • [ 18880-04-1 ]
  • [ 1213611-52-9 ]
  • 5
  • [ 150008-24-5 ]
  • [ 18880-04-1 ]
  • [ 1229313-30-7 ]
  • 6
  • [ 57473-33-3 ]
  • [ 18880-04-1 ]
  • [ 1366126-77-3 ]
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