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Merck
CN

15406

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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关于此项目

线性分子式:
(CH)3COCONH(CH2)5NH2
化学文摘社编号:
51644-96-3
分子量:
202.29
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
57647414
MDL number:
MFCD00210020
Beilstein/REAXYS Number:
3603658

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产品名称

N-Boc-尸胺, ≥97.0% (NT)

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)

SMILES string

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

InChI key

DPLOGSUBQDREOU-UHFFFAOYSA-N

assay

≥97.0% (NT)

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.460

density

0.972 g/mL at 20 °C (lit.)

functional group

Boc
amine

Quality Level

200

相关类别

Other Notes

制备聚胺和聚酰胺的结构单元

Application

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).

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109.0 °C - closed cup

ppe

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

法规信息

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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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V.J. Jasys et al.
The Journal of Organic Chemistry, 57, 1814-1814 (1992)
T. Teshima et al.
Tetrahedron, 47, 3305-3305 (1991)
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)
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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商品

MRT - Mono-Boc-Protection of Diamines

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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