640042
1-叔丁氧羰基-4-氨基哌啶
97%
别名:
1-Boc-4-氨基哌啶, 4-氨基-1-哌啶甲酸叔丁酯
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关于此项目
经验公式（希尔记法）:
C10H20N2O2
化学文摘社编号:
分子量:
200.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
SMILES string
CC(C)(C)OC(=O)N1CCC(N)CC1
InChI
1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-8(11)5-7-12/h8H,4-7,11H2,1-3H3
InChI key
LZRDHSFPLUWYAX-UHFFFAOYSA-N
Application
4-氨基-1-Boc-哌啶可用于：
- 作为合成N-（3-（4-羟苯基）-丙烯酰基）-氨基酸类色胺的原料，该产物可用作沉默信息调节剂人2型（SIRT2）抑制剂
- 合成哌啶取代的三嗪衍生物和哌啶基氨基-二芳基嘧啶（pDAPY）衍生物，这些衍生物可作为有效的HIV-1非核苷逆转录酶抑制剂（HIV-1 NNRTIs）
通过伯胺与树脂结合型二甲磺酸盐直接成环，用于N-取代哌啶的微波辅助固相合成。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Calum Macleod et al.
Journal of combinatorial chemistry, 8(1), 132-140 (2006-01-10)
The microwave-assisted solid-phase synthesis of piperazines, 3,9-diazaspiro[5.5]undecanes and 2,9-diazaspiro[5.5]undecanes is reported. The synthesis relies on the direct annulation of primary amines with resin-bound bismesylates. Critical to the success of this chemistry was the development of alpha-methyl benzyl carbamate resin linker.
"Novel piperidinylamino-diarylpyrimidine derivatives with dual structural conformations as potent HIV-1 non-nucleoside reverse transcriptase inhibitors"
Chen X, et al.
Bioorganic & Medicinal Chemistry, 23(24), 6593-6597 (2013)
"Synthesis and biological evaluation of piperidine-substituted triazine derivatives as HIV-1 non-nucleoside reverse transcriptase inhibitors"
Chen X, et al.
European Journal of Organic Chemistry, 51, 60- 66 (2012)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 640042-1G | 04061826291924 |
| 640042-5G | 04061833046111 |