(4-Chlorophenyl)(piperazin-1-yl) methanone
- CAS No.
- 54042-47-6
- Chemical Name:
- (4-Chlorophenyl)(piperazin-1-yl) methanone
- Synonyms
- 1-(4-CHLOROBENZOYL)PIPERAZINE;(4-Chlorophenyl)(piperazin-1-yl) methanone;Methanone, (4-chlorophenyl)-1-piperazinyl-
- CBNumber:
- CB5253201
- Molecular Formula:
- C11H13ClN2O
- Molecular Weight:
- 224.69
- MDL Number:
- MFCD01050442
- MOL File:
- 54042-47-6.mol
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H315-H335-H319-H302 |
| Precautionary statements | P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501 |
| Hazard Codes | Xn |
| Risk Statements | 22-36 |
(4-Chlorophenyl)(piperazin-1-yl) methanone price More Price(44)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Activate Scientific | AS114920 | (4-Chlorophenyl)(piperazin-1-yl)methanone 95% | 54042-47-6 | 1g | $156 | 2026-06-04 | Buy |
| Activate Scientific | AS114920 | (4-Chlorophenyl)(piperazin-1-yl)methanone 95% | 54042-47-6 | 5g | $489 | 2026-06-04 | Buy |
| Matrix Scientific | 305232 | (4-Chlorophenyl)(piperazin-1-yl)methanone | 54042-47-6 | 1.00g | $115 | 2026-05-19 | Buy |
| Matrix Scientific | 305232 | (4-Chlorophenyl)(piperazin-1-yl)methanone | 54042-47-6 | 5.00g | $361 | 2026-05-19 | Buy |
| Matrix Scientific | 305232 | (4-Chlorophenyl)(piperazin-1-yl)methanone | 54042-47-6 | 25.00g | $994 | 2026-05-19 | Buy |
(4-Chlorophenyl)(piperazin-1-yl) methanone Chemical Properties, Uses, Production
Synthesis
897445-35-1
54042-47-6
Step 2: Synthesis of (4-chlorophenyl)(piperazin-1-yl)methanone (C) Dissolve tert-butyl 4-(4-chlorobenzoyl)piperazine-1-carboxylate (26 g) in dichloromethane (350 mL). To the solution was added 4 M hydrochloric acid/dioxane solution (150 mL). The reaction mixture was stirred at room temperature for 4 hours, during which time the formation of a white precipitate was observed. Upon completion of the reaction, the mixture was concentrated to remove the solvent. The resulting white solid was washed with ether. Subsequently, the white solid was treated with 1 N sodium hydroxide solution (200 mL) and extracted with ethyl acetate (3 x 100 mL). The organic phases were combined, dried over anhydrous sodium sulfate and concentrated to give the target product (4-chlorophenyl)(piperazin-1-yl)methanone (17.79 g, 99% yield). Product characterization data: 1H-NMR (hydrochloride, 300 MHz, MeOD): δ 2.80-2.90 (m, 4H), 3.20-3.80 (m, 4H), 7.29-7.36 (m, 4H).
References
[1] Patent: WO2006/71875, 2006, A1. Location in patent: Page/Page column 78
[2] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 2, p. 1139 - 1148
[3] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 16, p. 3739 - 3743
[4] Archiv der Pharmazie, 2017, vol. 350, # 8,
[5] Patent: CN107226807, 2017, A. Location in patent: Paragraph 0546-0548


(4-Chlorophenyl)(piperazin-1-yl) methanone Preparation Products And Raw materials
Raw materials
Preparation Products
(4-Chlorophenyl)(piperazin-1-yl) methanone Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
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| Yuzhou Enthalpy Carbon Pharmaceutical Technology Co. LTD | 19963477321; 19963477321 | 2041275825@qq.com | China | 1541 | 58 |
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