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[ CAS No. 2439-54-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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| 2439-54-5
Chemical Structure| 2439-54-5
Structure of 2439-54-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2439-54-5 ]

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Product Citations

Product Details of [ 2439-54-5 ]

CAS No. :2439-54-5 MDL No. :MFCD00048927
Formula : C9H21N Boiling Point : No data available
Linear Structure Formula :- InChI Key :SEGJNMCIMOLEDM-UHFFFAOYSA-N
M.W : 143.27 Pubchem ID :75538
Synonyms :

Calculated chemistry of [ 2439-54-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 7
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.18
TPSA : 12.03 ?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) : -4.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.93
Log Po/w (XLOGP3) : 3.7
Log Po/w (WLOGP) : 2.57
Log Po/w (MLOGP) : 2.54
Log Po/w (SILICOS-IT) : 2.41
Consensus Log Po/w : 2.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.6
Solubility : 0.362 mg/ml ; 0.00253 mol/l
Class : Soluble
Log S (Ali) : -3.64
Solubility : 0.0326 mg/ml ; 0.000227 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.52
Solubility : 0.0438 mg/ml ; 0.000305 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.22

Safety of [ 2439-54-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2735
Hazard Statements:H227-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2439-54-5 ]

* 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 [ 2439-54-5 ]

[ 2439-54-5 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 111-25-1 ]
  • [ 2439-54-5 ]
  • hexyl-methyl-octyl-amine [ No CAS ]
  • 2
  • [ 2439-54-5 ]
  • [ 107-99-3 ]
  • [ 117685-18-4 ]
  • 3
  • [ 111-85-3 ]
  • [ 74-89-5 ]
  • [ 2439-54-5 ]
  • [ 4455-26-9 ]
  • 4
  • [ 111-83-1 ]
  • [ 74-89-5 ]
  • [ 2439-54-5 ]
YieldReaction ConditionsOperation in experiment
With potassium; In ethanol; (a) Preparation of N-methyl-N-octyl amine N-methyl-N-octyl amine is prepared in the following way: STR6 405 g of a 37percent methyl amine solution in ethanol and 150 g of n-octyl bromide were introduced into a 1 liter autoclave. The autoclave is heated to 180° C. for 20 hours and then to 200° C. for 8 hours. The crude residue is evaporated to dryness after cooling. Thus, a grey crystalline residue is obtained, which is treated with 300 ml of a 20percent potassium solution. The aqueous phase is extracted with ether, the ethereal phase is dried on magnesium sulphate, followed by filtration and expulsion of the ether. The sought product is then recoered with a good yield by distillation (approximately 70percent). The boiling point is 75° to 78° C., under 13 mmHg.
  • 7
  • [ 2439-54-5 ]
  • [ 56555-02-3 ]
  • N-Methyl-9-oxo-10-aza-octadecansaeure-methylester [ No CAS ]
  • 8
  • [ 63493-49-2 ]
  • [ 2439-54-5 ]
  • 9
  • [ 292638-84-7 ]
  • [ 50-00-0 ]
  • [ 2439-54-5 ]
  • [ 23580-89-4 ]
  • [ 87462-13-3 ]
  • 10
  • [ 17639-93-9 ]
  • [ 2439-54-5 ]
  • (S)-2-Chloro-N-methyl-N-octyl-propionamide [ No CAS ]
  • (R)-2-Chloro-N-methyl-N-octyl-propionamide [ No CAS ]
  • 11
  • [ 1942-45-6 ]
  • [ 2439-54-5 ]
  • Octyl-((E)-2-propyl-hex-2-enyl)-amine [ No CAS ]
  • 12
  • [ 2439-54-5 ]
  • [ 2835-68-9 ]
  • [ 66521-49-1 ]
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