1-(CYCLOPROPANECARBONYL)PIPERAZINE97
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1-(CYCLOPROPANECARBONYL)PIPERAZINE97
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CAS No:
59878-57-8
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Formula:
C8H14N2O
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Chemical Name:
1-(CYCLOPROPANECARBONYL)PIPERAZINE97
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Synonyms:
1-(CYCLOPROPANECARBONYL)PIPERAZINE97;1-(Cyclopropylcarbonyl)piperazine, 97%;Piperazine, 1-(cyclopropylcarbonyl)- (9CI);1-(Cyclopropylcarbonyl)piperazine hydrochloride 97%;Cyclopropyl(piperazin-1-yl)methan-1-one hydrochloride;Piperazine, 1-(cyclopropylcarbonyl)-;N-(Cyclopropylcarbonyl)piperazine;1-(Cyclopropylcarbonyl)piperazine, 97%colorless to pale brown liquid
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CAS No:
Characteristics
32.3
-0.5
Colorless to pale brown Liquid
1.087 g/mL at 25 °C
120 °C0.15 mm Hg
>230 °F
n20/D 1.524
Safety Information
NONH for all modes of transport
2
37/38-41
26-36/37/39
Xi
P261-P280-P305 + P351 + P338
H315-H318-H335
|Danger|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
1-(CYCLOPROPANECARBONYL)PIPERAZINE97 Use and Manufacturing
1-Tertbutoxycarbonyl-4-(cyclopropanecarbonyl) piperazine (190 mg, 0.75 mmol) was dissolved in dichloromethane, and then trifluoroacetic acid (1 mL) was added. The reaction mixture was stirred at room temperature until complete reaction, and then washed with saturated sodium bicarbonate solution for three times. The organic phases were concentrated to give 112 mg (yield 97percent) pale yellow solid of N-(cyclopropanecarbonyl) piperazine for use.1 -Tertbutoxycarbonyl-4-(cyclopropanecarbonyl)piperazine (190 mg, 0.75 mmol) was dissolved in dichloromethane, and then trifluoroacetic acid (1 mE) was added. The reaction mixture was stirred at room temperature until complete reaction, and then washed with saturated sodium bicarbonate solution for three times. The organic phases were concentrated to give 112mg (yield 97percent) pale yellow solid of N-(cyclopropanecarbonyl) piperazine for use.In 100 mL of ethanol was dissolved benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate (3.00 g, 10.4 mmol), and 1.5 g of 10percent palladium-carbon was added thereto, followed by stirring at room temperature under hydrogen atmosphere overnight. The palladium-carbon was removed by filtration, and the filtrate was evaporated to give the title compound (1.50 g, 97.3percent) as a colorless oil.1H-NMR Spectrum (CDCl3, 400MHz) δ(ppm): 0.73-0.80(2H, m), 0.96-1.03(2H, m), 1.67-1.77(1H, m), 2.82-2.97(4H, m), 3.60-3.71 (4H, m).10percent Palladium on carbon (175 mg, 10percent by wt.) was placed under an inert atmosphere and suspended in EtOH (5 mL). A solution of (4-benzyl-piperazin-1-yl)-cyclopropyl- methanone (1.75 g, 7.16 mmol) dissolved in EtOH (25 mL) was added. The reaction mixture was placed under H
Computed Properties
Molecular Weight:154.21
XLogP3:-0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:154.110613074
Monoisotopic Mass:154.110613074
Topological Polar Surface Area:32.3
Heavy Atom Count:11
Complexity:160
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1-(CYCLOPROPANECARBONYL)PIPERAZINE97
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