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[ CAS No. 33483-66-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 33483-66-8
Chemical Structure| 33483-66-8
Structure of 33483-66-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 33483-66-8 ]

CAS No. :33483-66-8 MDL No. :MFCD09991703
Formula : C7H16ClN Boiling Point : -
Linear Structure Formula :- InChI Key :GIRKJSRZELQHDX-UHFFFAOYSA-N
M.W : 149.66 Pubchem ID :12714125
Synonyms :

Calculated chemistry of [ 33483-66-8 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.32
TPSA : 26.02 Ų

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) : -5.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.33
Log Po/w (WLOGP) : 2.33
Log Po/w (MLOGP) : 1.83
Log Po/w (SILICOS-IT) : 1.32
Consensus Log Po/w : 1.56

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.24
Solubility : 0.87 mg/ml ; 0.00581 mol/l
Class : Soluble
Log S (Ali) : -2.52
Solubility : 0.457 mg/ml ; 0.00305 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.06
Solubility : 13.2 mg/ml ; 0.0879 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.1

Safety of [ 33483-66-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 33483-66-8 ]

* 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 [ 33483-66-8 ]

[ 33483-66-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1943-83-5 ]
  • [ 33483-66-8 ]
  • [ 33147-75-0 ]
  • 2
  • [ 33483-66-8 ]
  • [ 33185-87-4 ]
  • 3
  • [ 33483-66-8 ]
  • [ 2523-56-0 ]
YieldReaction ConditionsOperation in experiment
1.78 g To <strong>[33483-66-8]cis-4-methylcyclohexylamine hydrochloride</strong> (5.0 g), water and sodium bicarbonate were added, and the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off to prepare a free form of cis-4-methylcyclohexylamine (770 mg). 5 N hydrochloric acid was further added to the aqueous layer obtained above. PoraPak Rxn CX (ion-exchange resin, 30 g) was added thereto, and the mixture was left at room temperature. The resin was washed with deionized water, followed by elution with a 0.4 N ammonia/methanol solution. The eluate was concentrated to obtain a free form of cis-4-methylcyclohexylamine (1.01 g). The obtained free forms were combined (1.78 g).
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