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[ CAS No. 46460-73-5 ] {[proInfo.proName]}

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Chemical Structure| 46460-73-5
Chemical Structure| 46460-73-5
Structure of 46460-73-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 46460-73-5 ]

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Product Details of [ 46460-73-5 ]

CAS No. :46460-73-5 MDL No. :MFCD02094511
Formula : C11H16N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :JXWABCYGGVHAHB-UHFFFAOYSA-N
M.W : 208.26 Pubchem ID :417669
Synonyms :

Calculated chemistry of [ 46460-73-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 7
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 57.82
TPSA : 64.35 ?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) : -6.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 0.86
Log Po/w (WLOGP) : 1.11
Log Po/w (MLOGP) : 1.25
Log Po/w (SILICOS-IT) : 1.15
Consensus Log Po/w : 1.3

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.51
Solubility : 6.48 mg/ml ; 0.0311 mol/l
Class : Very soluble
Log S (Ali) : -1.79
Solubility : 3.34 mg/ml ; 0.016 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.4
Solubility : 0.082 mg/ml ; 0.000394 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.08

Safety of [ 46460-73-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 46460-73-5 ]

* 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 [ 46460-73-5 ]

[ 46460-73-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 1207-69-8 ]
  • [ 46460-73-5 ]
  • [ 85185-24-6 ]
  • [ 85185-22-4 ]
  • 2
  • [ 46460-73-5 ]
  • [ 85185-24-6 ]
  • [ 98577-76-5 ]
  • 3
  • [ 28170-07-2 ]
  • [ 109-76-2 ]
  • [ 46460-73-5 ]
  • 4
  • [ 69312-43-2 ]
  • [ 46460-73-5 ]
  • [ 702679-42-3 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20℃; To a solution of 1-methylethyl 2, 4-dichloropyrimidine-5-carboxylate (4.7 G) and ethyldiisopropylamine (3.4 ml) in ACETONITRILE (250 ML) phenylmethyl [3- AMINOPROPYL] CARBAMATE (4.2 g) was added at 0C. Subsequently the reaction mixture was stirred over night at room temperature. After evaporation the residue was chromatographed on SILICA GEL (DICHLOROMETHANE/ISOPROPANOL) to yield the title compound (5.9 G). ESI-MS : 407 and 409 (M+)
  • 5
  • [ 46460-73-5 ]
  • [ 107819-90-9 ]
  • [ 168827-62-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In N,N-dimethyl-formamide; at 20℃; for 72h; Method C, Step 1;, A mixture of N-Cbz-1,3-diaminopropane, hydrochloride (C1, 1.22 g) in DMF (15 mL) with triethylamine (1.4 mL) and then N,N-di(Boc)-S-methylurea (C2, 1.46 g) was stirred rt for 72 h. The reaction mixture was concentrated in vacuo to give a colorless residue which was purified using silica gel plates and elute with hexane:EtOAc C3 (1.65 g).
  • 6
  • [ 46460-73-5 ]
  • [ 3970-39-6 ]
  • benzyl (3-((2-methoxy-6-nitrophenyl)amino)propyl)carbamate [ No CAS ]
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