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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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$785.00

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1 ML
$216.00
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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编号:
MFCD00210020
UNSPSC代码:
12352200
PubChem化学物质编号:
57647414
NACRES:
NA.22

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质量水平

200

方案

≥97.0% (NT)

反应适用性

reagent type: cross-linking reagent

折射率

n20/D 1.460

密度

0.972 g/mL at 20 °C (lit.)

官能团

Boc
amine

SMILES字符串

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 key

DPLOGSUBQDREOU-UHFFFAOYSA-N

相关类别

应用

Some of the reported applications of N-Boc-cadaverine include:
  • Synthesis of of a supermacrocycle that self-assemble to form organic nanotubes.[1]
  • Preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye.[2]
  • Synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).[3]

其他说明

制备聚胺和聚酰胺的结构单元[4][5][6]

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

228.2 °F - closed cup

闪点(°C)

109.0 °C - closed cup

个人防护装备

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCB7735
BCBC8355V
BCBC8355
BCBS8337V
1356882

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T. Teshima et al.
Tetrahedron, 47, 3305-3305 (1991)
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
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)
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)
Helical rosette nanotubes: design, self-assembly, and characterization.
Fenniri H, et al.
Journal of the American Chemical Society, 123(16), 3854-3855 (2001)
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