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[ CAS No. 120205-50-7 ] {[proInfo.proName]}

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Chemical Structure| 120205-50-7
Chemical Structure| 120205-50-7
Structure of 120205-50-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 120205-50-7 ]

CAS No. :120205-50-7 MDL No. :MFCD18157735
Formula : C14H25NO5 Boiling Point : -
Linear Structure Formula :C9H17NO3C5H8O2 InChI Key :LNEHHTWYEBGHBY-OUAUKWLOSA-N
M.W : 287.35 Pubchem ID :11033491
Synonyms :
Chemical Name :(2R,3R)-3-((S)-1-(tert-Butoxycarbonyl)pyrrolidin-2-yl)-3-methoxy-2-methylpropanoic acid

Calculated chemistry of [ 120205-50-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 7
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 78.68
TPSA : 76.07 ?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) : -6.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.79
Log Po/w (XLOGP3) : 1.65
Log Po/w (WLOGP) : 1.74
Log Po/w (MLOGP) : 1.03
Log Po/w (SILICOS-IT) : 1.03
Consensus Log Po/w : 1.65

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.2
Solubility : 1.82 mg/ml ; 0.00632 mol/l
Class : Soluble
Log S (Ali) : -2.86
Solubility : 0.396 mg/ml ; 0.00138 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.97
Solubility : 30.4 mg/ml ; 0.106 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.85

Safety of [ 120205-50-7 ]

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 [ 120205-50-7 ]

* 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 [ 120205-50-7 ]

[ 120205-50-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 120205-50-7 ]
  • [ 135383-60-7 ]
  • [ 120205-54-1 ]
YieldReaction ConditionsOperation in experiment
81% With diethyl cyanophosphonate; triethylamine; In N,N-dimethyl-formamide; at 0 - 20℃; for 20.0h; To a solution of 11 (280 mg, 0.974 mmol, 1 eq.) and 15 (460 mg, 1.44 mmol, 1.48 eq.) in NN- dimethylformamide (3 mL, 0.32 M) at 0 C was added diethylphosphoryl cyanide (DEPC) (93% purity, 212 muEpsilon, 1.30 mmol, 1.34 eq.), followed by triethylamine (367 2.63 mmol, 2.7 eq.). After 2 hours at 0 C, the reaction mixture was warmed to room temperature for 18 hours. The reaction mixture was then diluted with ethyl acetate:toluene (2: 1, 30 mL) and was washed successively with 1 M aqueous sodium bisulfate solution (35 mL) and 50% saturated aqueous sodium bicarbonate solution (4 x 25 mL). The organic layer was dried over sodium sulfate, filtered, concentrated in vacuo, and purified by silica gel chromatography (12% to 100% ethyl acetate in heptane) to give 16 as a light amber oil (374 mg, 81%). LC-MS: m/z 474.4 [M+H+], 374.4 [(M - 2-methylprop-l-ene)+H+] retention time = 3.63 minutes; H NMR (400 MHz, DMSO-i), characteristic signals: delta 8.66 (d, J=8.5 Hz, IH), 7.78 (d, J=3.3 Hz, IH), 7.64 (d, J=3.3 Hz, IH), 7.21-7.31 (m, 4H), 7.14-7.20 (m, IH), 5.40 (ddd, J=1 1.4, 8.5, 4.0 Hz, IH), 3.23 (br s, 3H), 2.18 (dq, J=9.7, 6.7 Hz, IH), 1.06 (d, J=6.6 Hz, 3H).
  • 3
  • [ 120205-50-7 ]
  • [ 745017-94-1 ]
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