ChemicalBook--->CAS DataBase List--->68104-62-1

68104-62-1

68104-62-1 Structure

68104-62-1 Structure
IdentificationMore
[Name]

1-(4-BROMOPHENYL)PIPERAZINE HYDROCHLORIDE
[CAS]

68104-62-1
[Synonyms]

1-(4-BROMOPHENYL)-PIPERAZINE HCL
1-(4-BROMOPHENYL)PIPERAZINE HYDROCHLORIDE
RARECHEM AH CK 0050
1-(4-Bromophenyl)piperazine hydrochloride 98%
1-(4-Bromophenyl)-piperazine x HCl
1-(4-Bromophenyl)piperazin HCl
[Molecular Formula]

C10H14BrClN2
[MDL Number]

MFCD00674134
[Molecular Weight]

277.59
[MOL File]

68104-62-1.mol
Chemical PropertiesBack Directory
[Melting point ]

>280°C (dec.)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO: 10 mg/ml; PBS (pH 7.2): 10 mg/ml
[Water Solubility ]

Soluble in water
[form ]

powder to crystal
[color ]

White to Almost white
[InChI]

InChI=1S/C10H13BrN2.ClH/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13;/h1-4,12H,5-8H2;1H
[InChIKey]

YDVSFRZKQMQPJD-UHFFFAOYSA-N
[SMILES]

C1(C=CC(Br)=CC=1)N1CCNCC1.Cl
[CAS DataBase Reference]

68104-62-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HS Code ]

2933.59.8000
Hazard InformationBack Directory
[Description]

1-(4-Bromophenyl)piperazine hydrochloride is an important organic synthetic intermediate, playing a crucial role, especially in medicinal chemistry. It is not typically used as a final product, but rather introduced as a structural unit (i.e., a "building block") into more complex molecules to construct drug molecules with specific biological activities. The "p-bromophenyl" and "piperazine ring" contained in its structure are common pharmacophores in many central nervous system drugs, such as antipsychotics and antidepressants.
[Uses]

1-(4-Bromophenyl)piperazine Hydrochloride is useful in the synthesis of large bifunctional heterocycles use in targeted degradation of rapidly accelerated fibrosarcoma polypeptides
[Synthesis]

P-Bromoaniline undergoes a biphilic nucleophilic substitution reaction with bis(2-chloroethyl)amine in the presence of a base (e.g., sodium carbonate) to directly generate 1-(4-bromophenyl)piperazine. Finally, 1-(4-bromophenyl)piperazine reacts with hydrochloric acid to synthesize 1-(4-bromophenyl)piperazine hydrochloride.
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