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17354

Sigma-Aldrich

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
Beilstein:
2325117
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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P. Mougenot et al.
The Journal of Organic Chemistry, 61, 408-408 (1996)
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Convergent Synthesis and Diversity of Amino Acid Based Dendrimers
Arwin J B, et al.
European Journal of Organic Chemistry, 1903-1915 (2001)
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International journal of nanomedicine, 6, 2007-2021 (2011-10-07)
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Harmicines represent hybrid compounds composed of β-carboline alkaloid harmine and cinnamic acid derivatives (CADs). In this paper we report the synthesis of amide-type harmicines and the evaluation of their biological activity. N-harmicines 5a-f and O-harmicines 6a-h were prepared by a

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