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[ CAS No. 4138-26-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4138-26-5
Chemical Structure| 4138-26-5
Structure of 4138-26-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4138-26-5 ]

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Product Citations

Product Details of [ 4138-26-5 ]

CAS No. :4138-26-5 MDL No. :MFCD00005993
Formula : C6H12N2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :BVOCPVIXARZNQN-UHFFFAOYSA-N
M.W : 128.17 Pubchem ID :92980
Synonyms :

Calculated chemistry of [ 4138-26-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.47
TPSA : 55.12 ?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) : -7.98 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : -1.26
Log Po/w (WLOGP) : -0.91
Log Po/w (MLOGP) : -0.41
Log Po/w (SILICOS-IT) : 0.23
Consensus Log Po/w : -0.26

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.23
Solubility : 215.0 mg/ml ; 1.68 mol/l
Class : Highly soluble
Log S (Ali) : 0.6
Solubility : 509.0 mg/ml ; 3.97 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.64
Solubility : 29.4 mg/ml ; 0.229 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.67

Safety of [ 4138-26-5 ]

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

Application In Synthesis of [ 4138-26-5 ]

* 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 [ 4138-26-5 ]

[ 4138-26-5 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 25334-23-0 ]
  • [ 4138-26-5 ]
  • 2
  • [ 98-92-0 ]
  • [ 4138-26-5 ]
YieldReaction ConditionsOperation in experiment
98.4% With hydrogen;palladium 10% on activated carbon; In isopropyl alcohol; at 75℃; under 3750.38 Torr; for 4h; 122.12 g (1.00 mol) of nicotinamide was dissolved in 500 mL of 2-propanol. To the resulting solution was charged 14.4 g of palladium-carbon (10percent), and the solution was stirred for 4 hours at 75° C. under hydrogen pressure of 0.5 MPa. After the reaction was completed, the palladium-carbon was filtered and separated. The filtered palladium-carbon was washed with 100 mL of 2-propanol. The filtrate and the washing liquid were combined and condensed, and 126.08 g of white crystals of nipecotamide in a racemic form was obtained. The yield was 98.4percent. The resultant was confirmed to be the target object by NMR.
  • 3
  • [ 4138-26-5 ]
  • [ 67402-86-2 ]
  • [ 110454-61-0 ]
  • [ 110392-27-3 ]
  • 4
  • [ 4138-26-5 ]
  • [ 64516-58-1 ]
  • [ 110454-64-3 ]
  • [ 110392-28-4 ]
  • 5
  • [ 4138-26-5 ]
  • [ 72279-14-2 ]
  • [ 72279-00-6 ]
  • 6
  • [ 4138-26-5 ]
  • [ 79286-73-0 ]
  • [ 92242-67-6 ]
  • 7
  • [ 4138-26-5 ]
  • [ 89122-62-3 ]
  • [ 89122-53-2 ]
  • 9
  • [ 4138-26-5 ]
  • [ 1026307-84-5 ]
  • 1-[2-(6,11-Dioxo-6,11-dihydro-dibenzo[b,e]azepin-5-yl)-acetyl]-piperidine-3-carboxylic acid amide [ No CAS ]
  • 10
  • [ 4138-26-5 ]
  • [ 88585-79-9 ]
  • [ 166187-15-1 ]
  • 11
  • [ 4138-26-5 ]
  • [ 50-00-0 ]
  • 3-Carbamoyl-1-methylene-piperidinium; chloride [ No CAS ]
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