추천 제품
Quality Level
분석
99%
양식
liquid
refractive index
n20/D 1.541 (lit.)
bp
134 °C/7 mmHg (lit.)
density
1.021 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
O=C1CCN(CC1)Cc2ccccc2
InChI
1S/C12H15NO/c14-12-6-8-13(9-7-12)10-11-4-2-1-3-5-11/h1-5H,6-10H2
InChI key
SJZKULRDWHPHGG-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1-Benzyl-4-piperidone serves as a versatile heterocyclic building block in the synthesis of pharmaceutical compounds.
애플리케이션
1-Benzyl-4-piperidone is generally used as a building block in the synthesis of various medicinal compounds. Applications include the synthesis of:
- Spirocyclic furopyridines as haloperidol-sensitive σ receptor ligands.
- Multi-target-directed donepezil + propargylamine + 8-hydroxyquinoline (DPH) hybrids for the treatment of Alzheimer′s disease.
- Spiropiperidine iminohydantoin aspartyl protease inhibitors.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
159.8 °F
Flash Point (°C)
71 °C
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis and ? receptor affinity of regioisomeric spirocyclic furopyridines.
Miyata K, et al.
European Journal of Medicinal Chemistry, 83(2), 709-716 (2014)
Donepezil+ propargylamine+ 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimer's disease.
Wang Li, et al.
European Journal of Medicinal Chemistry, 80(2), 543-561 (2014)
Novel spiropiperidines as highly potent and subtype selective ?-receptor ligands. Part 1.
Maier CA and Wunsch B
Journal of Medicinal Chemistry, 45(2), 438-448 (2002)
Di-tert-butylsilylene-directed α-selective synthesis of 4-methylumbelliferyl T-antigen.
Imamura A, et al.
Organic Letters, 7(20), 4415-4418 (2005)
Chunmei Gao et al.
Bioorganic & medicinal chemistry, 16(18), 8670-8675 (2008-08-21)
A novel series of 10-benzyl-9(10H)-acridinones and 1-benzyl-4-piperidones were synthesized and tested for their in vitro antitumor activities against CCRF-CEM cells. Assay-based antiproliferative activity study using CCRF-CEM cell lines revealed that the acridone group and the substitution pattern on the benzene
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