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[ CAS No. 6306-61-2 ] N-(2-Chloroethyl)propan-2-amine hydrochloride

Cat. No.: A131310
Chemical Structure| 6306-61-2
Chemical Structure| 6306-61-2
Structure of 6306-61-2 * Storage: Inert atmosphere,2-8°C
Purity Size Price USA Stock *0-1 Day Global Stock *5-7 Days Quantity
95% 100mg $20.00 Inquiry Inquiry
95% 250mg $24.00 Inquiry Inquiry
95% 1g $50.00 Inquiry Inquiry
95% 5g $148.00 Inquiry Inquiry
95% 25g $520.00 Inquiry Inquiry

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Product Details of [ 6306-61-2 ]

CAS No. :6306-61-2 MDL No. :MFCD00034904
Formula : C5H13Cl2N Boiling Point : -
Linear Structure Formula :- InChI Key :SFRKVRBYLCHDBI-UHFFFAOYSA-N
M.W : 158.07 Pubchem ID :24183019
Synonyms :

Calculated chemistry of [ 6306-61-2 ]      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 : 1.0
Molar Refractivity : 40.71
TPSA : 12.03 Ų

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) : -5.85 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.99
Log Po/w (WLOGP) : 2.03
Log Po/w (MLOGP) : 1.89
Log Po/w (SILICOS-IT) : 1.15
Consensus Log Po/w : 1.41

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.88
Solubility : 2.1 mg/ml ; 0.0133 mol/l
Class : Very soluble
Log S (Ali) : -1.87
Solubility : 2.14 mg/ml ; 0.0135 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.13
Solubility : 1.16 mg/ml ; 0.00736 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 6306-61-2 ]

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 [ 6306-61-2 ]

* 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 [ 6306-61-2 ]

[ 6306-61-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1346133-39-8 ]
  • [ 6306-61-2 ]
  • [ 1346242-81-6 ]
YieldReaction ConditionsOperation in experiment
Intermediate 3 (20. Og; 55.3mmol), then tetra-N-butylammonium bromide (9.06g;27.7mmol) were added at 2C under inert atmosphere to a solution of potassium hydroxide (46.6g; 830mmol) in THF (387ml_) and water (6ml_). The reaction was stirred at room temperature for 2 hours before portionwise addition of N-(2-chloroethyl)-2- propanamine HCI (CAS[6306-61 -2]), and then at 50C upon complete conversion. Water was added, layers were separated and the organic layer concentrated, taken up in DCM/water, neutralized with HCI to neutral pH. Organic layer was washed with water, dried (MgS04), filtered and evaporated till dryness to give 26.6g of compound 4.
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