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[ CAS No. 27483-92-7 ] {[proInfo.proName]}

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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| 27483-92-7
Chemical Structure| 27483-92-7
Structure of 27483-92-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 27483-92-7 ]

CAS No. :27483-92-7 MDL No. :MFCD09800596
Formula : C7H15Cl2N Boiling Point : -
Linear Structure Formula :- InChI Key :AZZOFXGSQFRBCS-UHFFFAOYSA-N
M.W : 184.11 Pubchem ID :12644392
Synonyms :

Calculated chemistry of [ 27483-92-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
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 : 52.22
TPSA : 3.24 ?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) : -5.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.57
Log Po/w (WLOGP) : 2.13
Log Po/w (MLOGP) : 2.15
Log Po/w (SILICOS-IT) : 1.9
Consensus Log Po/w : 1.75

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.53
Solubility : 0.538 mg/ml ; 0.00292 mol/l
Class : Soluble
Log S (Ali) : -2.29
Solubility : 0.953 mg/ml ; 0.00517 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.76
Solubility : 3.19 mg/ml ; 0.0173 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.23

Safety of [ 27483-92-7 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P280-P301+P310+P330-P305+P351+P338-P337+P313-P405-P501 UN#:2811
Hazard Statements:H301-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 27483-92-7 ]

* 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 [ 27483-92-7 ]

[ 27483-92-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20845-34-5 ]
  • [ 27483-92-7 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In ethanol; chloroform; The 1-methylpiperidin-2-ylmethyl chloride hydrochloride used as a starting material was prepared as follows: Hydrogen chloride gas was bubbled into a solution of 1-methyl-2-piperidinemethanol (12.9 g) in chloroform (80 ml) until two layers developed. The resultant mixture was heated to reflux and thionyl chloride (29 ml) was added slowly. The mixture was stirred and heated to reflux for a further hour. The mixture was evaporated, ethanol was added and the mixture was re-evaporated. The residue was dissolved in ethanol and the solution was decolourised with charcoal. The clear filtrate was diluted with diethyl ether until turbidity occurred. The required compound (12 g) crystallized from the solution; m.p. 159-162° C.; Mass: M+H+147.
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