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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:
39684-80-5
Molecular Weight:
224.10
Beilstein/REAXYS Number:
2325117
MDL number:
MFCD02683428
UNSPSC Code:
12352101
PubChem Substance ID:
57647641
NACRES:
NA.22

Quality Level

200

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

Related Categories

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
GHS07

signalword

Warning

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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