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[ CAS No. 125552-89-8 ] {[proInfo.proName]}

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Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 125552-89-8
Chemical Structure| 125552-89-8
Structure of 125552-89-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 125552-89-8 ]

CAS No. :125552-89-8 MDL No. :MFCD03788561
Formula : C6H11BrO Boiling Point : No data available
Linear Structure Formula :- InChI Key :LMOOYAKLEOGKJR-UHFFFAOYSA-N
M.W : 179.05 Pubchem ID :2773286
Synonyms :

Calculated chemistry of [ 125552-89-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.8
TPSA : 9.23 ?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) : -6.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.15
Log Po/w (XLOGP3) : 1.58
Log Po/w (WLOGP) : 1.81
Log Po/w (MLOGP) : 1.66
Log Po/w (SILICOS-IT) : 2.43
Consensus Log Po/w : 1.93

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.88
Solubility : 2.36 mg/ml ; 0.0132 mol/l
Class : Very soluble
Log S (Ali) : -1.38
Solubility : 7.39 mg/ml ; 0.0412 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.03
Solubility : 1.66 mg/ml ; 0.00927 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.16

Safety of [ 125552-89-8 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P264-P280-P301+P310+P330+P331-P303+P361+P353+P310-P304+P340+P310-P305+P351+P338+P310-P363-P405-P501 UN#:3265
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 125552-89-8 ]

* 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 [ 125552-89-8 ]

[ 125552-89-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 125552-89-8 ]
  • [ 5932-27-4 ]
  • [ 1309785-28-1 ]
  • [ 1309785-30-5 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In acetonitrile; at 20℃; for 18.5h; To a solution of ethyl 1 H-pyrazole-3-carboxylate (2 g) in MeCN (40 ml) was added cesium carbonate (4.65 g) and the mixture stirred for 30 min when 4-(bromomethyl)tetrahydro-2H- pyran (2.81 g) was added and the mixture stirred at RT for 18 h. The solvent was removed in vacuo and the residue partitioned between dichloromethane (50 ml) and water (20 ml), separated by hydrophobic frit and concentrated. The filtrate was purified by silica (2 x 100 g) cartridge on Flashmaster II using a gradient of DCM and ethyl acetate to give the title compound 1 as a colourless oil, 0.944 g and title compound 2, as a colourless oil, 1 .026g.1 ; LCMS (method B); Rt = 0.90 min, MH+ = 239.2; LCMS (method B); Rt = 0.75 min, MH+ = 239.
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