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15406

Sigma-Aldrich

N-Boc-尸胺

≥97.0% (NT)

别名:

N-(5-氨戊基)氨基甲酸叔丁酯, N-Boc-1,5-戊二胺

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About This Item

线性分子式:
(CH)3COCONH(CH2)5NH2
CAS号:
51644-96-3
分子量:
202.29
Beilstein:
3603658
MDL號碼:
MFCD00210020
分類程式碼代碼:
12352200
PubChem物質ID:
57647414
NACRES:
NA.22

品質等級

200

化驗

≥97.0% (NT)

反應適用性

reagent type: cross-linking reagent

折射率

n20/D 1.460

密度

0.972 g/mL at 20 °C (lit.)

官能基

Boc
amine

SMILES 字串

NCCCCCNC(OC(C)(C)C)=O

InChI

1S/C10H22N2O2/c1-10(2,3)14-9(13)12-8-6-4-5-7-11/h4-8,11H2,1-3H3,(H,12,13)

InChI 密鑰

DPLOGSUBQDREOU-UHFFFAOYSA-N

相关类别

應用

Some of the reported applications of N-Boc-cadaverine include:
  • Synthesis of of a supermacrocycle that self-assemble to form organic nanotubes.
  • Preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye.
  • Synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).

其他說明

制备聚胺和聚酰胺的结构单元

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H314

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

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C Melchiorre et al.
Journal of medicinal chemistry, 32(1), 79-84 (1989-01-01)
Several polymethylene tetraamines related to methoctramine (1) were prepared and evaluated for their blocking activity on M-2 muscarinic receptors in guinea pig atria and ileum. It turned out that antimuscarinic potency depends on the following parameters: (a) nature of the
T. Teshima et al.
Tetrahedron, 47, 3305-3305 (1991)
Helical rosette nanotubes: design, self-assembly, and characterization.
Fenniri H, et al.
Journal of the American Chemical Society, 123(16), 3854-3855 (2001)
A toolset of functionalized porphyrins with different linker strategies for application in bioconjugation.
Staegemann M H, et al.
Organic & Biomolecular Chemistry, 14(38), 9114-9132 (2016)
Rapid Synthesis of Unsymmetrical Sulforhodamines Through Nucleophilic Amination of a Monobrominated Sulfoxanthene Dye.
Chevalier A, et al.
European Journal of Organic Chemistry, 2015(1), 152-165 (2015)
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