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[ CAS No. 13374-30-6 ] {[proInfo.proName]}

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Chemical Structure| 13374-30-6
Chemical Structure| 13374-30-6
Structure of 13374-30-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13374-30-6 ]

CAS No. :13374-30-6 MDL No. :MFCD09259963
Formula : C6H14ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :LKKCSUHCVGCGFA-GEMLJDPKSA-N
M.W : 151.63 Pubchem ID :11715205
Synonyms :

Calculated chemistry of [ 13374-30-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
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 : 39.68
TPSA : 46.25 ?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) : -6.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.74
Log Po/w (WLOGP) : 1.05
Log Po/w (MLOGP) : 0.57
Log Po/w (SILICOS-IT) : 0.39
Consensus Log Po/w : 0.55

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.25
Solubility : 8.6 mg/ml ; 0.0567 mol/l
Class : Very soluble
Log S (Ali) : -1.29
Solubility : 7.77 mg/ml ; 0.0512 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.1
Solubility : 122.0 mg/ml ; 0.802 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.97

Safety of [ 13374-30-6 ]

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

Application In Synthesis of [ 13374-30-6 ]

* 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 [ 13374-30-6 ]

[ 13374-30-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 34619-03-9 ]
  • [ 13374-30-6 ]
  • (+-)-trans-2-N-(tert-butoxycarbonyl)-cyclohexanol [ No CAS ]
  • [ 121282-70-0 ]
YieldReaction ConditionsOperation in experiment
5.86 g (96%) With sodium hydrogencarbonate; In dichloromethane; Step A (+-)-trans-2-(tert-Butoxycarbonylamino)-cyclohexanol To a vigoursly stirring solution of trans-2-aminocyclohexanol hydrochloride (5.5 g, 36 mmol) in 100 mL methylene chloride and saturated sodium bicarbonate solution (1:1) at 0 C. was added di-tert-butylcarbonate (13.09 g, 60 mmol). The resulting heterogeneous mixture was warmed to the room temperature and stirred overnight. The methylene chloride layer was washed with brine, dried and evaporated. The solid obtained was triturated with hexane and filtered to give 5.86 g (96%) of (+-)-trans-2-N-(tert-butoxycarbonyl)-cyclohexanol. 1 H NMR (500 MHz, CDCl3): delta4.61(brs, 1H), 3.27 (m, 1H), 2.73 (brs, 1H), 2.02-1.69 (m, 4H), 1,45 (s, 9H), 1.42-1.09(m, 4H). 13 C NMR (125 MHz, CDCl3): delta75.42, 56.62, 34.22, 31.84, 28.43, 27.48, 24.78, 24.11.
  • 2
  • [ 24424-99-5 ]
  • [ 13374-30-6 ]
  • [ 121282-70-0 ]
YieldReaction ConditionsOperation in experiment
88% With triethylamine; In dichloromethane; at 20℃; for 2h; To a stirred suspension of (lS,2S)-(+)-2-aminocyclohexanol hydrochloride (1.04 g, 6.86 mmol) in DCM (20 mL) was added triethylamine (2.39 mL, 17.1 mmol). A solution of di-tert-butyl dicarbonate (1.80 g, 8.23 mmol) in DCM (15 mL) was added dropwise. The reaction mixture was stirred at ambient temperature for 2 hours. The reaction was diluted with DCM and washed successively with IN HC1, saturated aqueous NaHCC"3 and brine, dried and concentrated. The residue was purified by column chromatography (hexane/EtOAc, 1 : 1) to give tert-butyl (l S,2S)-2- hydroxycyclohexylcarbamate (1.30 g, 88%).
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