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[ CAS No. 34839-14-0 ] {[proInfo.proName]}

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Chemical Structure| 34839-14-0
Chemical Structure| 34839-14-0
Structure of 34839-14-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 34839-14-0 ]

CAS No. :34839-14-0 MDL No. :MFCD11113550
Formula : C3H9Cl2NO Boiling Point : -
Linear Structure Formula :- InChI Key :ZCPJBHYNOFIAPJ-DFWYDOINSA-N
M.W : 146.02 Pubchem ID :87178124
Synonyms :

Calculated chemistry of [ 34839-14-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 32.17
TPSA : 46.25 ?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) : -7.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.06
Log Po/w (WLOGP) : 0.35
Log Po/w (MLOGP) : 0.23
Log Po/w (SILICOS-IT) : -0.07
Consensus Log Po/w : 0.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.65
Solubility : 32.6 mg/ml ; 0.223 mol/l
Class : Very soluble
Log S (Ali) : -0.58
Solubility : 38.0 mg/ml ; 0.26 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.36
Solubility : 64.3 mg/ml ; 0.441 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.0

Safety of [ 34839-14-0 ]

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

Application In Synthesis of [ 34839-14-0 ]

* 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 [ 34839-14-0 ]

[ 34839-14-0 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 34839-14-0 ]
  • [ 110-13-4 ]
  • [ 1429334-14-4 ]
YieldReaction ConditionsOperation in experiment
17.5 g With sodium acetate; for 2.0h;Reflux; To a solution of (2S)-3-chloro-2-hydroxypropylamine.HCl (14.6 g, 0.1 mol) ( prepared in Ex.1) and Sodium acetate ( 16.4 g, 0.2 mol) in acetic acid (150 ml) was added 2,5- hexanedione (12.54g, 0.1 1 mol) and then refluxed for 2 hrs. Pour the R.M into water (500 ml) and then extracted with DCM (100 ml x3 ). Washed DCM layer with sat. aq. Sodium bicarbonate solution ( 50 ml x 2) and water ( 50 ml x 2) . Distill- off the solvent under reduced pressure to yield title compound (Yield = 17.5 g, 92.2% of the theory).
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