17354
2-(Boc-amino)ethyl bromide
≥97.0% (GC)
Synonym(s):
N-Boc-2-bromoethyl-amine, tert-Butyl N-(2-bromoethyl)carbamate
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About This Item
Linear Formula:
BrCH2CH2NHCO2C(CH3)3
CAS Number:
Molecular Weight:
224.10
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2325117
Assay:
≥97.0% (GC)
Quality Level
assay
≥97.0% (GC)
reaction suitability
reagent type: cross-linking reagent
mp
30-32 °C (lit.)
functional group
Boc, amine, bromo
shipped in
wet ice
storage temp.
−20°C
SMILES string
BrCCNC(OC(C)(C)C)=O
InChI
1S/C7H14BrNO2/c1-7(2,3)11-6(10)9-5-4-8/h4-5H2,1-3H3,(H,9,10)
InChI key
TZRQZPMQUXEZMC-UHFFFAOYSA-N
General description
2-(Boc-amino)ethyl bromide is used in organic synthesis to introduce Boc-protective group and enable the synthesis of various compounds like peptides.
Other Notes
Building block for preparing fluorinated spacers having nucleophilic and electrophilic termini; synthesis of a biphenyl linker
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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L. Chen et al.
Tetrahedron Letters, 39, 3627-3627 (1998)
Convergent Synthesis and Diversity of Amino Acid Based Dendrimers
Arwin J B, et al.
European Journal of Organic Chemistry, 1903-1915 (2001)
Jinping Cheng et al.
International journal of nanomedicine, 6, 2007-2021 (2011-10-07)
Carbon nanotubes have shown broad potential in biomedical applications, given their unique mechanical, optical, and chemical properties. In this pilot study, carbon nanotubes have been explored as multimodal drug delivery vectors that facilitate antiangiogenic therapy in zebrafish embryos. Three different
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 17354-1G | 04061838062284 |
| 17354-5G | 04061838751942 |