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[ CAS No. 5211-23-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5211-23-4
Chemical Structure| 5211-23-4
Structure of 5211-23-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 5211-23-4 ]

CAS No. :5211-23-4 MDL No. :MFCD00134246
Formula : C14H17NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :BLQYEDXWEDWCNJ-LBPRGKRZSA-N
M.W : 263.29 Pubchem ID :688168
Synonyms :
1,2-Pyrrolidinedicarboxylic acid, 2-methyl 1-(phenylmethyl) ester, (S)-;Methyl (S)-N-(benzyloxycarbonyl)prolinate
Chemical Name :(S)-1-Benzyl 2-methyl pyrrolidine-1,2-dicarboxylate

Calculated chemistry of [ 5211-23-4 ]

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.71
TPSA : 55.84 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.85
Log Po/w (XLOGP3) : 1.74
Log Po/w (WLOGP) : 1.43
Log Po/w (MLOGP) : 1.57
Log Po/w (SILICOS-IT) : 1.55
Consensus Log Po/w : 1.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.41
Solubility : 1.03 mg/ml ; 0.00392 mol/l
Class : Soluble
Log S (Ali) : -2.53
Solubility : 0.778 mg/ml ; 0.00296 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.79
Solubility : 0.432 mg/ml ; 0.00164 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.84

Safety of [ 5211-23-4 ]

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

Application In Synthesis of [ 5211-23-4 ]

* 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.

  • Upstream synthesis route of [ 5211-23-4 ]
  • Downstream synthetic route of [ 5211-23-4 ]

[ 5211-23-4 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 5211-23-4 ]
  • [ 22348-32-9 ]
Reference: [1] Journal of Organic Chemistry, 1988, vol. 53, # 12, p. 2861 - 2863
  • 2
  • [ 5211-23-4 ]
  • [ 34381-71-0 ]
Reference: [1] Journal of the American Chemical Society, 1987, vol. 109, # 23, p. 7111 - 7115
  • 3
  • [ 5211-23-4 ]
  • [ 2133-40-6 ]
Reference: [1] Advanced Synthesis and Catalysis, 2007, vol. 349, # 4-5, p. 535 - 538
  • 4
  • [ 5211-23-4 ]
  • [ 92053-25-3 ]
Reference: [1] Journal of the American Chemical Society, 1990, vol. 112, # 19, p. 6936 - 6942
  • 5
  • [ 5211-23-4 ]
  • [ 118971-00-9 ]
Reference: [1] Journal of the American Chemical Society, 1990, vol. 112, # 19, p. 6936 - 6942
  • 6
  • [ 5211-23-4 ]
  • [ 110529-22-1 ]
Reference: [1] Journal of the American Chemical Society, 1987, vol. 109, # 23, p. 7111 - 7115
  • 7
  • [ 5211-23-4 ]
  • [ 110529-22-1 ]
Reference: [1] Journal of the Chemical Society, Chemical Communications, 1987, # 6, p. 467 - 468
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