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[ CAS No. 5407-04-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5407-04-5
Chemical Structure| 5407-04-5
Structure of 5407-04-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5407-04-5 ]

CAS No. :5407-04-5 MDL No. :MFCD00012521
Formula : C5H13Cl2N Boiling Point : -
Linear Structure Formula :(CH3)2NCH2CH2CH2Cl·HCl InChI Key :LJQNMDZRCXJETK-UHFFFAOYSA-N
M.W : 158.07 Pubchem ID :94308
Synonyms :
Chemical Name :3-Chloro-N,N-dimethylpropan-1-amine hydrochloride

Calculated chemistry of [ 5407-04-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.81
TPSA : 3.24 ?2

Pharmacokinetics

GI absorption : Low
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) : -5.84 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.01
Log Po/w (WLOGP) : 1.98
Log Po/w (MLOGP) : 1.89
Log Po/w (SILICOS-IT) : 0.87
Consensus Log Po/w : 1.35

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.89
Solubility : 2.04 mg/ml ; 0.0129 mol/l
Class : Very soluble
Log S (Ali) : -1.71
Solubility : 3.12 mg/ml ; 0.0197 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.77
Solubility : 2.66 mg/ml ; 0.0168 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.4

Safety of [ 5407-04-5 ]

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 [ 5407-04-5 ]

* 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 [ 5407-04-5 ]

[ 5407-04-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5791-00-4 ]
  • [ 5407-04-5 ]
  • 6-chloro-4-(3-dimethylamino-propyl)-2-methyl-4<i>H</i>-benzo[1,4]oxazin-3-one [ No CAS ]
  • 2
  • [ 5407-04-5 ]
  • [ 56741-95-8 ]
  • 5-bromo-2-<(3-dimethylamino)propylamino>-6-phenyl-4(3H)-pyrimidinone [ No CAS ]
  • 3
  • [ 539-15-1 ]
  • [ 5407-04-5 ]
  • [ 325151-65-3 ]
  • 4
  • [ 5407-04-5 ]
  • [ 939-69-5 ]
  • 6-(3-dimethylaminopropoxy)-2-cyanobenzothiazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With potassium carbonate; sodium iodide; In acetone;Reflux; The mixture of 6-hydroxy-2-cyanobenzothiozole(0.311 g, 1.77 mmol), 3-chloropropyldimethylamine hydrochloride (0.36 g, 2.27 mmol), potassium carbonate (0.63g, 4.57 mmol) and sodium iodide (0.034 g) in acetone (30 ml) was heated to reflux overnight. Upon cooling to roomtemperature, the insoluble solid was removed by filtration. The compound was purified by flash chromatography usingmethylene chloride/methanol (96:4) as eluent in a yield of 86percent (0.387 g).1H NMR (CD2Cl2): 7.98 (d, J= 9.3 Hz, 1H), 7.32 (d, J= 2.4 Hz, 1H), 7.16 (dd, J = 9.0 Hz, J= 2.1 Hz, 1H), 4.04 (t, J = 6.4Hz, 2H, OCH2), 2.36 (t, J = 7.2 Hz, 2H, NCH2), 2.13 (s, 6H, CH3), 1.90 (m, 2H, CH2).
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