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[ CAS No. 13504-86-4 ] {[proInfo.proName]}

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Chemical Structure| 13504-86-4
Chemical Structure| 13504-86-4
Structure of 13504-86-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 13504-86-4 ]

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Product Details of [ 13504-86-4 ]

CAS No. :13504-86-4 MDL No. :MFCD00238423
Formula : C13H15NO5 Boiling Point : -
Linear Structure Formula :- InChI Key :WWVCWLBEARZMAH-QWRGUYRKSA-N
M.W : 265.26 Pubchem ID :688414
Synonyms :
Chemical Name :(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acid

Calculated chemistry of [ 13504-86-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.38
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 69.55
TPSA : 87.07 ?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) : -7.38 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 0.76
Log Po/w (WLOGP) : 0.31
Log Po/w (MLOGP) : 0.5
Log Po/w (SILICOS-IT) : 0.14
Consensus Log Po/w : 0.67

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.87
Solubility : 3.6 mg/ml ; 0.0136 mol/l
Class : Very soluble
Log S (Ali) : -2.17
Solubility : 1.8 mg/ml ; 0.00679 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.28
Solubility : 14.0 mg/ml ; 0.0528 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.1

Safety of [ 13504-86-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501 UN#:
Hazard Statements:H302-H312-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13504-86-4 ]

* 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.

  • Downstream synthetic route of [ 13504-86-4 ]
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