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2-Phenylpiperazine

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Products Intro: Product Name:2-Phenylpiperazine
CAS: 5271-26-1
Purity:90%-99.9% Package:1KG;USD
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Products Intro: Product Name:2-Phenylpiperazine
CAS:5271-26-1

2-Phenylpiperazine manufacturers

  • 2-Phenylpiperazine
  • 2-Phenylpiperazine  pictures
  • $1.10 / 1g
  • 2025-11-18
  • CAS:5271-26-1
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons
  • 2-Phenylpiperazine
  • 2-Phenylpiperazine pictures
  • $0.00 / 1KG
  • 2019-07-07
  • CAS: 5271-26-1
  • Min. Order: 1KG
  • Purity: 90%-99.9%
  • Supply Ability: 500kg
2-Phenylpiperazine Basic information
Product Name:2-Phenylpiperazine
Synonyms:m-phenylpiperazine;2-PHENYLPIPERAZINE;2-Phenylpiperazine 97%;Piperazine, 2-phenyl-;2-Phenylpiperazine ISO 9001:2015 REACH;2-Phenylpiperizine
CAS:5271-26-1
MF:C10H14N2
MW:162.23
EINECS:627-379-0
Product Categories:pharmacetical;Piperaizine;Piperazine derivates;Building Blocks;Heterocyclic Building Blocks;Piperazines
Mol File:5271-26-1.mol
2-Phenylpiperazine Structure
2-Phenylpiperazine Chemical Properties
Melting point 83-87 °C (lit.)
Boiling point 138 °C
density 0.997±0.06 g/cm3(Predicted)
storage temp. Storage temp. 2-8°C
form solid
pka8.80±0.40(Predicted)
color Yellow
InChI1S/C10H14N2/c1-2-4-9(5-3-1)10-8-11-6-7-12-10/h1-5,10-12H,6-8H2
InChIKeyRIMRLBGNCLMSNH-UHFFFAOYSA-N
SMILESC1CNC(CN1)c2ccccc2
CAS DataBase Reference5271-26-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36/37
RIDADR UN3259
WGK Germany 2
Hazard Note Irritant
HazardClass 8
HS Code 29335990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
2-Phenylpiperazine Usage And Synthesis
Uses2-Phenylpiperazine is the starting material for the synthesis of 2-phenylpiperazine compounds. It has been synthesized 1,4-dimethyl-2-phenylpiperazine, 1,4-diethyl-2-phenyl Piperazine etc.
Synthesis
3-Phenylpiperazin-2-one

5368-28-5

2-Phenylpiperazine

5271-26-1

General procedure for the synthesis of 2-phenylpiperazine from 3-oxo-2-phenylpiperazine: 2-oxo-3-phenylpiperazine (1.76 g, 10 mmol) was dissolved in 30 mL of anhydrous THF and added slowly and dropwise to 20 mL (20 mmol) of a THF solution of 1M LiAlH4. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, water and 20% NaOH solution were carefully added to quench the excess LiAlH4. Subsequently, the reaction mixture was filtered and the filter cake was re-extracted with ethyl acetate. The organic filtrate and extract were combined, dried with MgSO4, filtered and concentrated under reduced pressure to give a light yellow solid. The crude product was further purified by silica gel column chromatography (eluent: CHCl3:MeOH:NH4OH = 9:1:0.1) to afford 2-phenylpiperazine (960 mg, 6 mmol, 60% yield) as a colorless solid. The product was characterized by 1H NMR (CDCl3): δ 2.69 (1H, t, J = 11.3 Hz), 2.85-3.10 (7H, m), 3.76 (1H, br d, J = 8.9 Hz), 7.21-7.38 (5H, m). Melting point determination (capillary method): 79-81°C.

References[1] Patent: WO2004/63150, 2004, A2. Location in patent: Page 28-29
[2] Patent: US2005/222166, 2005, A1. Location in patent: Page/Page column 13
[3] Patent: EP1396487, 2004, A1. Location in patent: Page 17-18
2-Phenylpiperazine Preparation Products And Raw materials
Raw materials3-Phenylpiperazin-2-one-->Piperazine, 2-phenyl-1,4-bis(phenylmethyl)--->Lithium Aluminum Hydride-->Tetrahydrofuran
Tag:2-Phenylpiperazine(5271-26-1) Related Product Information
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