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[ CAS No. 5382-17-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5382-17-2
Chemical Structure| 5382-17-2
Structure of 5382-17-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5382-17-2 ]

Related Doc. of [ 5382-17-2 ]

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Product Citations

Product Details of [ 5382-17-2 ]

CAS No. :5382-17-2 MDL No. :MFCD00035298
Formula : C5H12ClNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :VKCORPXOKYDINR-UHFFFAOYSA-N
M.W : 137.61 Pubchem ID :16212499
Synonyms :

Calculated chemistry of [ 5382-17-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.88
TPSA : 32.26 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.47
Log Po/w (WLOGP) : 0.15
Log Po/w (MLOGP) : 0.21
Log Po/w (SILICOS-IT) : 0.73
Consensus Log Po/w : 0.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.99
Solubility : 14.1 mg/ml ; 0.103 mol/l
Class : Very soluble
Log S (Ali) : -0.72
Solubility : 26.4 mg/ml ; 0.192 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.44
Solubility : 50.3 mg/ml ; 0.366 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 5382-17-2 ]

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

Application In Synthesis of [ 5382-17-2 ]

* 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 [ 5382-17-2 ]

[ 5382-17-2 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 151-50-8 ]
  • [ 108-94-1 ]
  • [ 5382-17-2 ]
  • [ 60756-86-7 ]
  • 2
  • [ 5382-17-2 ]
  • [ 814-68-6 ]
  • 1-(4-hydroxypiperidine)prop-2-en-1-one [ No CAS ]
  • 3
  • [ 13734-34-4 ]
  • [ 5382-17-2 ]
  • [ 186431-51-6 ]
  • 4
  • [ 5382-17-2 ]
  • [ 41153-30-4 ]
  • [ 186431-68-5 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In DMF (N,N-dimethyl-formamide); at 20℃; for 16.0h; To a stirred solution OF BOC-3- (4-FLUOROPHENYL)- (S)-ALANINE (LO. OG, 35. 3MMOL), <strong>[5382-17-2]4-hydroxypiperidine hydrochloride</strong> (5. 1G, 37. 1MMOL) and HOBt (7.2g, 52. 9MMOL) in DMF (lOOmL), was added DIPEA (12. 3mL, 70. 6MMOL) and after 5MIN, EDCI (7.4g, 38. 8MMOL) and the reaction stirred at rt for 16H. The solvent was removed in vacuo and the residue partitioned between water (150ML) and ethyl acetate (2 x 150ML). The combined organic fractions were washed with sodium hydroxide solution (2M, 50ML), hydrochloric acid (2N, 50ML), dried (MGS04) and concentrated in vacuo. The product was chromatographed on silica gel eluting with ethyl acetate to give the title compound as a white solid. m/z (ES+) = 367 [M+ H] + ; RT = 3.28min.
  • 5
  • [ 13414-95-4 ]
  • [ 5382-17-2 ]
  • 1-(4,5,6,7-Tetrahydro-benzo[b]thiophen-4-yl)-piperidin-4-ol [ No CAS ]
  • 6
  • [ 5382-17-2 ]
  • [1-chloro-4-(3-chloro-4-methoxybenzyl)amino]-6-[4-14C]phthalazinecarbonitrile [ No CAS ]
  • C21(14)CH22ClN5O2 [ No CAS ]
  • 7
  • [ 24424-99-5 ]
  • [ 5382-17-2 ]
  • [ 109384-19-2 ]
  • 8
  • [ 506-68-3 ]
  • [ 5382-17-2 ]
  • [ 51075-37-7 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In dichloromethane; water; at 0℃; for 1.08333h; Preparation 11: 4-Hydroxypiperidine-l-carbonitrileA stirred slurry OfNa2CO3 (9.8 g, 117 mmol) in water (15 mL) was cooled on ice-water and 4-hydroxypiperidine.HCl (4.0 g, 29.2 mmol) was added. A solution of cyanogen bromide(3.7 g, 35 mmol) in CH2Cl2 (90 mL) was added portionwise over 5 min and the stirring continued for 1 h. The reaction was diluted with CH2Cl2 ( 100 mL), the organic phase separated and dried (MgSO-O and the solvent evaporated to afford the title cyanamide: SH (CDCl3) 1.65 (ddt, 2H), 1.91 (ddt, 2H), 2.17 (br s, IH), 3.08 (ddd, 2H), 3.45 (ddd, 2H), 3.86 (sept, IH).
  • 9
  • [ 5198-49-2 ]
  • [ 5382-17-2 ]
  • 1-[2-(4-chlorophenylamino)ethyl]piperidin-4-ol [ No CAS ]
  • 10
  • [ 5382-17-2 ]
  • [ 73775-92-5 ]
  • 11
  • [ 5382-17-2 ]
  • N-[18F]Fluoroethyl-4-piperidyl acetate [ No CAS ]
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