15502
1-Boc-哌嗪
≥98.0% (GC)
别名:
哌嗪-1-甲酸叔丁酯
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关于此项目
经验公式（希尔记法）:
C9H18N2O2
化学文摘社编号:
分子量:
186.25
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
879985
Assay:
≥98.0% (GC)
Form:
solid
Quality Level
assay
≥98.0% (GC)
form
solid
mp
43-47 °C
SMILES string
CC(C)(C)OC(=O)N1CCNCC1
InChI
1S/C9H18N2O2/c1-9(2,3)13-8(12)11-6-4-10-5-7-11/h10H,4-7H2,1-3H3
InChI key
CWXPZXBSDSIRCS-UHFFFAOYSA-N
Application
1-Boc-哌嗪与各种芳基卤化物发生 Buchwald-Hartwig 胺化反应，形成相应的的胺衍生物。它可用于合成许多生物活性分子的单取代哌嗪中间体和含有哌嗪的原料药，如曲唑酮。
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Conformationally rigid derivatives of WAY-267,464: Synthesis and pharmacology at the human oxytocin and vasopressin-1a receptors.
Jorgensen WT, et al.
European Journal of Medicinal Chemistry, 143, 1644-1656 (2018)
Discovery of 1-[2-(2, 4-dimethylphenylsulfanyl) phenyl] piperazine (Lu AA21004): a novel multimodal compound for the treatment of major depressive disorder.
Bang-Andersen B, et al.
Journal of Medicinal Chemistry, 54(9), 3206-3221 (2011)
Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1 H-benzo [d] imidazol-2 (3 H)-ones.
Ullah N
Journal of Enzyme Inhibition and Medicinal Chemistry, 29(2), 281-291 (2014)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 15502-25G | 04061833416600 |
| 15502-5G | 04061833355008 |