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[ CAS No. 2133-40-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2133-40-6
Chemical Structure| 2133-40-6
Structure of 2133-40-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2133-40-6 ]

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Product Citations

Product Details of [ 2133-40-6 ]

CAS No. :2133-40-6 MDL No. :MFCD00012708
Formula : C6H12ClNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HQEIPVHJHZTMDP-JEDNCBNOSA-N
M.W : 165.62 Pubchem ID :2733200
Synonyms :
Chemical Name :H-Pro-OMe.HCl

Calculated chemistry of [ 2133-40-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.81
TPSA : 38.33 ?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) : -6.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.91
Log Po/w (WLOGP) : 0.33
Log Po/w (MLOGP) : 0.35
Log Po/w (SILICOS-IT) : 0.63
Consensus Log Po/w : 0.45

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.31
Solubility : 8.15 mg/ml ; 0.0492 mol/l
Class : Very soluble
Log S (Ali) : -1.3
Solubility : 8.29 mg/ml ; 0.0501 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.85
Solubility : 23.5 mg/ml ; 0.142 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.85

Safety of [ 2133-40-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2133-40-6 ]

* 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 [ 2133-40-6 ]

[ 2133-40-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2133-40-6 ]
  • [ 3290-06-0 ]
  • [ 221392-56-9 ]
YieldReaction ConditionsOperation in experiment
With tetra-(n-butyl)ammonium iodide; potassium carbonate; In water; N,N-dimethyl-formamide; a (+-)-Methyl N-(3,5-dichlorobenzyl)prolinate To methyl prolinate HCl (0.5 g), K2CO3 (1.25 g) and 3,5-dichlorobenzylchloride (0.59 g) in DMF (5 mL) was added tetrabutylammonium iodide (cat). The solution was stirred overnight, water was added, and the mixture was extracted with ethyl acetate. The organic layer was dried (Na2SO4), solvent was removed under reduced pressure, and silica gel flash chromatography (0.5percent methanol/CH2Cl2) yielded the desired product (0.65 g). ES(+) MS m/e=288.3 (M+H).
  • 2
  • [ 5779-93-1 ]
  • [ 2133-40-6 ]
  • methyl (2,3-dimethylbenzyl)-L-prolinate [ No CAS ]
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