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[ CAS No. 67622-86-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 67622-86-0
Chemical Structure| 67622-86-0
Structure of 67622-86-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 67622-86-0 ]

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Product Details of [ 67622-86-0 ]

CAS No. :67622-86-0 MDL No. :MFCD11043099
Formula : C5H13NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :KYCZVVFGMGLNPL-UHFFFAOYSA-N
M.W : 103.16 Pubchem ID :13432442
Synonyms :

Calculated chemistry of [ 67622-86-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 30.15
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) : -7.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.69
Log Po/w (XLOGP3) : -0.27
Log Po/w (WLOGP) : -0.02
Log Po/w (MLOGP) : 0.23
Log Po/w (SILICOS-IT) : -0.13
Consensus Log Po/w : 0.3

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.18
Solubility : 68.6 mg/ml ; 0.664 mol/l
Class : Very soluble
Log S (Ali) : 0.05
Solubility : 116.0 mg/ml ; 1.13 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.9
Solubility : 13.0 mg/ml ; 0.126 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 67622-86-0 ]

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

Application In Synthesis of [ 67622-86-0 ]

* 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 [ 67622-86-0 ]

[ 67622-86-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 558-42-9 ]
  • [ 74-89-5 ]
  • [ 67622-86-0 ]
YieldReaction ConditionsOperation in experiment
In methanol; at 100℃; for 0.25h;Microwave irradiation; EXAMPLE 121 4-[2-tert-Butyl-1-(tetrahydropyran-4-ylmethyl)-1H-imidazol-4-yl]-N-(2-hydroxy-2-methylpropyl)-N-methylthiophene-2-carboxamide (Compound 121) Step 1; 1-Chloro-2-methyl-2-propanol (103 muL, 1.00 mmol) was dissolved in a 40percent methylamine methanol solution (0.5 mL), and the mixture was stirred at 100°C for 15 minutes at 100 W in a microwave-assisted chemical synthesis instrument (CEM Discover). After the mixture was left to cool to room temperature, the solvent was evaporated under reduced pressure. Then, acetonitrile (3 mL) was added to the residue, and the precipitated solid was removed by filtration. After an aqueous sodium hydrogen carbonate solution (10 drops) was added to the filtrate, the solvent was evaporated under reduced pressure to give a roughly purified product of 2-methyl-1-(methylamino)propan-2-ol. The roughly purified product was used in the subsequent step as such without purification.
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