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1-(4-?????)????

1-(4-?????)????
1-(4-?????)???? ??? ???
?? ??:
66698-28-0
???:
1-(4-?????)????
???(??):
1-(4-?????)????
???:
1-(4-Bromophenyl)piperazine
???(??):
KML-30;CML-027;1-(4-Bromophenyl);1-(4-BROMOPHENYL)PIPERAZINE;Piperazine, 1-(4-bromophenyl)-;1-(4-Bromophenyl)piperazine - [B93256];1-(4-BROMO-PHENYL)-PIPERAZINE DIHYDROCHLORIDE
CBNumber:
CB8389893
???:
C10H13BrN2
??? ??:
241.13
MOL ??:
66698-28-0.mol
MSDS ??:
SDS

1-(4-?????)???? ??

???
91-95 °C
?? ?
353.3±27.0 °C(Predicted)
??
1.386±0.06 g/cm3(Predicted)
?? ??
2-8°C
?? ?? (pKa)
8.88±0.10(Predicted)
??? ??
solid
InChI
InChI=1S/C10H13BrN2/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8H2
InChIKey
PJHPFAFEJNBIDC-UHFFFAOYSA-N
SMILES
N1(C2=CC=C(Br)C=C2)CCNCC1
CAS ??????
66698-28-0(CAS DataBase Reference)

??

??? ?? Xi,Xn
?? ???? ?? 20/21/22
WGK ?? 1
?? ?? ?? Irritant
???? ??? 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral

1-(4-?????)???? C??? ??, ??, ??

??

1-(4-Bromophenyl)piperazine (street names: 4-bromo-piperein, 4-BP, brein) is structurally related to 1-(4-fluorophenyl)piperazine and to 1-(4-chlorophenyl)piperazine. The only difference is the halogen substituent type attached to the phenyl ring's para-position. In the case of NPSs from the methcathinone group, which are also neurotransmitter releasers, structure–activity studies demonstrated that the replacement of a fluorine or chlorine atom with a bromine atom resulted in a compound with more potency for the release of both dopamine and serotonin. The lowest dopamine selectivity, an additional consequence of these halogen replacements, results in lower abuse potential in favor of empathogenic properties[1].

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