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Merck
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文件

15404

Sigma-Aldrich

N-Boc-1,4-丁二胺

≥97.0% (GC/NT)

同義詞:

N-(4-氨丁基)氨基甲酸叔丁酯, N-Boc-1,4-二氨基丁烷

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About This Item

線性公式:
(CH3)3COCONH(CH2)4NH2
CAS號碼:
分子量::
188.27
Beilstein:
1937878
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥97.0% (GC/NT)

反應適用性

reagent type: cross-linking reagent

折射率

n20/D 1.460

密度

0.984 g/mL at 20 °C (lit.)

官能基

Boc
amine

SMILES 字串

NCCCCNC(OC(C)(C)C)=O

InChI

1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)

InChI 密鑰

ZFQWJXFJJZUVPI-UHFFFAOYSA-N

應用

  • 羧基-硅烷涂覆氧化铁纳米颗粒:详述采用N-Boc-1,4-丁二胺修饰氧化铁纳米颗粒用于成像和药物递送(D Stanicki, S Boutry, S Laurent, et al., 2014)。访问文章

其他說明

药理活性化合物的制备。亚精胺类似物的制备。C4-间隔基的引入。

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

228.2 °F - closed cup

閃點(°C)

109.0 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


分析證明 (COA)

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文章

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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