556017
N-Boc-4-哌啶甲醇
97%
别名:
N-叔丁氧羰基-4-哌啶甲醇
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关于此项目
经验公式（希尔记法）:
C11H21NO3
化学文摘社编号:
分子量:
215.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
InChI
1S/C11H21NO3/c1-11(2,3)15-10(14)12-6-4-9(8-13)5-7-12/h9,13H,4-8H2,1-3H3
SMILES string
CC(C)(C)OC(=O)N1CCC(CO)CC1
InChI key
CTEDVGRUGMPBHE-UHFFFAOYSA-N
assay
97%
form
solid
mp
78-82 °C (lit.)
functional group
hydroxyl
General description
N-Boc-4-哌啶甲醇含有一个叔丁氧羰基(t-BOC)-保护基团。可由4-哌啶甲醇与焦碳酸二叔丁酯反应合成。
Application
N-Boc-4-哌啶甲醇可用于合成：
- 5-甲氧基-4-(1-甲基哌啶-4-基甲氧基)-2-硝基苯甲酸甲酯
- N-Boc-4-哌啶醛
- [1-(叔丁氧羰基)哌啶-4-基]甲磺酸甲酯
参与减慢心率药合成。
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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Seimbille Y, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 48(11), 829-843 (2005)
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European journal of medicinal chemistry, 44(1), 124-130 (2008-04-29)
We describe here the synthesis and the binding interaction with sigma(1) and sigma(2) receptors of a series of new benzo[d]oxazol-2(3H)-one derivatives variously substituted on the N-benzyl moiety. The results of binding studies confirm the notion that the benzoxazolone moiety confers
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