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Merck
CN

641472

Sigma-Aldrich

1-Boc-4-(氨基甲基)哌啶

97%

别名:

1,1-Dimethylethyl 4-(aminomethyl)-1-piperidinecarboxylate, N-(tert-Butoxycarbonyl)-4-aminomethylpiperidine

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About This Item

经验公式(希尔记法):
C11H22N2O2
分子量:
214.30
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

折射率

n20/D 1.473 (lit.)

沸点

237-238 °C (lit.)

密度

1.013 g/mL at 25 °C (lit.)

官能团

amine

SMILES字符串

CC(C)(C)OC(=O)N1CCC(CN)CC1

InChI

1S/C11H22N2O2/c1-11(2,3)15-10(14)13-6-4-9(8-12)5-7-13/h9H,4-8,12H2,1-3H3

InChI key

KLKBCNDBOVRQIJ-UHFFFAOYSA-N

应用

Precursor in the preparation of a variety of different protein agonists or antagonists including:
  • Kinesin spindle protein inhibitors with potential anticancer activity
  • Orphan G-protein coupled receptor GPR119 agonist with antidiabetic potential
  • Pim-1 inhibitors
  • Aspartic acid protease inhibitors

Reactant involved in enantioselective synthesis of N-alkyl terminal aziridines

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

No data available

闪点(°C)

No data available

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.

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