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[ CAS No. 73579-08-5 ] {[proInfo.proName]}

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Chemical Structure| 73579-08-5
Chemical Structure| 73579-08-5
Structure of 73579-08-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 73579-08-5 ]

CAS No. :73579-08-5 MDL No. :MFCD00006498
Formula : C7H16N2 Boiling Point : No data available
Linear Structure Formula :CH3N(CH2CH2)2CHNHCH3 InChI Key :XRYGCVVVDCEPRL-UHFFFAOYSA-N
M.W : 128.22 Pubchem ID :566323
Synonyms :

Calculated chemistry of [ 73579-08-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.26
TPSA : 15.27 ?2

Pharmacokinetics

GI absorption : Low
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) : -6.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.09
Log Po/w (XLOGP3) : 0.39
Log Po/w (WLOGP) : -0.08
Log Po/w (MLOGP) : 0.57
Log Po/w (SILICOS-IT) : 0.61
Consensus Log Po/w : 0.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.81
Solubility : 19.6 mg/ml ; 0.153 mol/l
Class : Very soluble
Log S (Ali) : -0.28
Solubility : 67.8 mg/ml ; 0.529 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.16
Solubility : 8.85 mg/ml ; 0.069 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.12

Safety of [ 73579-08-5 ]

Signal Word:Danger Class:8,3
Precautionary Statements:P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P403+P235-P405 UN#:2920
Hazard Statements:H225-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 73579-08-5 ]

* 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 [ 73579-08-5 ]

[ 73579-08-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73579-08-5 ]
  • [ 97-08-5 ]
  • [ 211915-77-4 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In pyridine; water; a 4-Chloro-3-nitrobenzenesulphonic acid-N-(1-methyl-piperidin-4-yl)-N-methyl-amide To a solution of 2.2 ml (15 mMol) of 1-methyl-4-methylamino-piperidine in 60 ml pyridine, 3.8 g (15 mMol) of 4-chloro-3-nitro-benzenesulphonic acid chloride were added, in batches, whilst cooling with ice. The mixture was then stirred for two hours with cooling, then evaporated to dryness, the residue was mixed with about 50 ml of water and made alkaline with concentrated ammonia whilst stirring vigorously. The crude product precipitated was suction filtered and purified by column chromatography (250 g silica gel, eluant: dichloromethane with 1.5% ethanol). Yield: 1.6 g (31% of theory), C13 H18 ClN3 O4 S (347.8) Rf value: 0.19 (silica gel; dichloromethane/ethanol=19:1)
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