trans-1-Cinnamylpiperazine

Names

[ Name ]:
trans-1-Cinnamylpiperazine

[Synonym ]:
4-[(2E)-3-PHENYLPROP-2-EN-1-YL]PIPERIDINE
MFCD00063251
EINECS 242-652-0
1-[(2E)-3-phenylprop-2-en-1-yl]piperazine
1-cinnamylpiperazine
1-[(2e)-3-phenylprop-2-en-1-yl]piperazin
(E)-4-(3-phenyl-2-propenyl)piperazine
1-TRANS-CINNAMYL PIPERAZINE
1-PHENYL-3-(1-PIPERAZINO)-1-PROPENE
1-(3-phenyl-2-propenyl)piperazine
1-(3-PHENYL-ALLYL)-PIPERAZINE
trans-1-cinnamyl piperazine
TRANS-1-CINNAMYL-PIPERAZINE
trans-1-Cinnamylpiperazine
((2E)-3-phenylprop-2-enyl)piperazine
1-(3-Phenyl-2-propenyl)piperazin
1-[(E)-3-phenylallyl]-piperazine
TRANS-1-CINNAMYLPIPERAZIN
Piperazine, 1-[(2E)-3-phenyl-2-propen-1-yl]-
1-CINNAMYL PIPERAZINE
N-CINNAMYLPIPERAZINE
1-[(2E)-3-Phenyl-2-propen-1-yl]piperazine
trans-1-Ciamylpiperazine

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
341.7±30.0 °C at 760 mmHg

[ Melting Point ]:
39-44 °C(lit.)

[ Molecular Formula ]:
C₁₃H₁₈N₂

[ Molecular Weight ]:
202.295

[ Flash Point ]:
151.2±15.5 °C

[ Exact Mass ]:
202.147003

[ PSA ]:
15.27000

[ LogP ]:
2.05

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.569

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

In vitro efficacy of new antiprotozoals against Philasterides dicentrarchi (Ciliophora, Scuticociliatida).

Dis. Aquat. Organ. 62(1-2) , 97-102, (2004)

Philasterides dicentrarchi is a histiophagous ciliate that causes severe losses in turbot and sea bass farming. This study investigated the in vitro efficacy against P. dicentrarchi of 85 newly synthe...

Structure–activity relationship studies of the chromosome segregation inhibitor, Incentrom A

Bioorg. Med. Chem. Lett. 18(16) , 4670-4, (2008)

Pharmacophore and structure–activity relationship of Incentrom A that inhibits the chromosome segregation process in yeast were established. A series of Incentrom A analogs were synthesized and tested...