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[ CAS No. 19962-04-0 ] {[proInfo.proName]}

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Chemical Structure| 19962-04-0
Chemical Structure| 19962-04-0
Structure of 19962-04-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 19962-04-0 ]

CAS No. :19962-04-0 MDL No. :MFCD00052699
Formula : C9H12N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :LKEQZFMJKLCAEA-UHFFFAOYSA-N
M.W : 180.20 Pubchem ID :29877
Synonyms :

Calculated chemistry of [ 19962-04-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.44
TPSA : 55.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.68 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.9
Log Po/w (XLOGP3) : 1.02
Log Po/w (WLOGP) : 1.34
Log Po/w (MLOGP) : 1.19
Log Po/w (SILICOS-IT) : 0.1
Consensus Log Po/w : 1.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.74
Solubility : 3.25 mg/ml ; 0.0181 mol/l
Class : Very soluble
Log S (Ali) : -1.78
Solubility : 3.02 mg/ml ; 0.0167 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.84
Solubility : 2.62 mg/ml ; 0.0146 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.92

Safety of [ 19962-04-0 ]

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 [ 19962-04-0 ]

* 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 [ 19962-04-0 ]

[ 19962-04-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19962-04-0 ]
  • [ 77-78-1 ]
  • [ 51-60-5 ]
YieldReaction ConditionsOperation in experiment
84.6% With calcium carbonate; In acetone; at 25 - 30℃; A clean and dry 1000 ml 4 neck round bottom flask was charged with 3- aminophenyl dimethyl carbamate (50 gm), Calcium carbonate (50 gm) and acetone (300 ml). The reaction mixture was stirred for 5 min. Dimehtyl sulphate (128.3 gm) was added to the reaction mixture and stirred at 25 " 30eC for 16 " 18 hours. The reaction completion was confirmed by T LC analysis. (0197) The reaction mixture was filtered to remove calcium carbonate. Later cooled to 0 " 5 · C and solid thus formed was collected to afford crude compound which was crystallized from isopropanol to provide pure neostigmine methyl sulfate. (0198) Y ield : 81 gm (84.6 %) (0199) M P : 142 - 145 - C
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