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[ CAS No. 132945-75-6 ] {[proInfo.proName]}

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Chemical Structure| 132945-75-6
Chemical Structure| 132945-75-6
Structure of 132945-75-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 132945-75-6 ]

CAS No. :132945-75-6 MDL No. :MFCD09953436
Formula : C10H19NO5S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 265.33 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 132945-75-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 66.64
TPSA : 81.29 ?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) : -7.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.4
Log Po/w (XLOGP3) : 0.73
Log Po/w (WLOGP) : 1.67
Log Po/w (MLOGP) : 0.64
Log Po/w (SILICOS-IT) : -0.26
Consensus Log Po/w : 1.04

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.61
Solubility : 6.44 mg/ml ; 0.0243 mol/l
Class : Very soluble
Log S (Ali) : -2.02
Solubility : 2.56 mg/ml ; 0.00964 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.05
Solubility : 23.6 mg/ml ; 0.0891 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.44

Safety of [ 132945-75-6 ]

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 [ 132945-75-6 ]

* 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 [ 132945-75-6 ]

[ 132945-75-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35344-95-7 ]
  • [ 132945-75-6 ]
  • (R)-tert-butyl 3-(4-formyl-1H-pyrazol-1-yl)pyrrolidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
91% With caesium carbonate; In N,N-dimethyl-formamide; at 100℃; for 18h; A mixture of <strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> (400 mg, 4.17 mmol), (S)-tert-butyl 3-(methylsulfonyloxy)pyrrolidine-1-carboxylate (1.21 g, 4.58 mmol) and Cs2CO3 (4.08 g, 12.51 mmol) in DMF (30 mL) was stirred at 100° C. for 18 hours. Solvent was removed in vacuo, and the residue was purified by silica gel column (pet ether:EtOAc 2:1) to give the desired product (R)-tert-butyl 3-(4-formyl-1H-pyrazol-1-yl)pyrrolidine-1-carboxylate as a colorless oil (1.0 g). Yield 91percent (ESI 266.0 (M+H)+).
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