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[ CAS No. 122536-94-1 ] {[proInfo.proName]}

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Chemical Structure| 122536-94-1
Chemical Structure| 122536-94-1
Structure of 122536-94-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 122536-94-1 ]

CAS No. :122536-94-1 MDL No. :MFCD00272298
Formula : C4H10ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :QPMSJEFZULFYTB-WCCKRBBISA-N
M.W : 123.58 Pubchem ID :22309122
Synonyms :

Calculated chemistry of [ 122536-94-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 34.07
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) : -6.98 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.11
Log Po/w (WLOGP) : -0.24
Log Po/w (MLOGP) : -0.16
Log Po/w (SILICOS-IT) : 0.52
Consensus Log Po/w : 0.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.68
Solubility : 26.1 mg/ml ; 0.211 mol/l
Class : Very soluble
Log S (Ali) : -0.34
Solubility : 56.1 mg/ml ; 0.454 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.13
Solubility : 91.4 mg/ml ; 0.74 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.37

Safety of [ 122536-94-1 ]

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

Application In Synthesis of [ 122536-94-1 ]

* 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 [ 122536-94-1 ]

[ 122536-94-1 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 501-53-1 ]
  • [ 122536-94-1 ]
  • [ 100858-32-0 ]
  • [ 100858-33-1 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In water; a) Preparation of benzyl (S)-3-hydroxy-pyrrolidine-1-carboxylate The pH of a solution of 6.18 g of (S)-3-hydroxy-pyrrolidine hydrochloride in 175 ml of water was adjusted to 10 with 10% sodium hydroxide solution and cooled to 0-5 C. 7.1 ml of benzyl chloroformate were added dropwise within 30 minutes under argon, with the pH of the solution being held between 9.5 and 11.5 by the dropwise addition of 10% sodium hydroxide solution. After completion of the addition the suspension was stirred at room temperature for 16 hours. The suspension was extracted with ethyl acetate, the organic phase was washed with water, dried over Na2 SO4, filtered and the filtrate was concentrated. Purification of the crude product over a silica gel column gave 7.33 g of benzyl (R)-3-hydroxy-pyrrolidine-1-carboxylate as a beige liquid.
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